Organic Halides

<p>2-Amino-1-(4-fluorophenyl)-1-propanone (Fluoroamphetamine) is a chemical that binds to the serotonin transporter, which is responsible for the reuptake of serotonin into the presynaptic neuron. Fluoroamphetamine has been shown to lower empathy and increase feelings of reward in animals. This drug has no significant effect on dopamine and noradrenaline levels but does cause an increase in metabolic acidosis. Fluoroamphetamine is most often used by analytical laboratories as a synthetic intermediate, but it can also be used as a strategy to develop specific antidotes against serotonin blockers. Fluoroamphetamine's health effects are similar to those of amphetamine with regards to cardiovascular risks and addictive potential.</p>

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<p>1,1-Dichlorodimethyl ether is a chemical compound that is used as an intermediate in the synthesis of trifluoroacetic acid from hydrochloric acid and methanol. This chemical has also been shown to inhibit inflammation by inhibiting the release of inflammatory cytokines, including epidermal growth factor (EGF) and interleukin-8 (IL-8). It may be used to treat chronic cough and chronic bronchitis. 1,1-Dichlorodimethyl ether inhibits the production of EGF by blocking the binding of EGF to its receptor on the surface of cells. The molecule also has an inhibitory effect on IL-8 production via inhibition of protein kinase C. The 1,1-dichlorodimethyl group is a reactive oxygen species that can react with other molecules such as DNA or proteins, leading to damage or even cell death.</p>

<p>Please enquire for more information about 3-Amino-5-bromobenzonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Bromopropionyl chloride is an organic compound that contains a hydroxyl group and a bromine atom, which are attached to the same carbon atom. It is used as a synthetic intermediate in the ring-opening polymerization of ethylene oxide. 2-Bromopropionyl chloride has been shown to be active against tumour cell lines, but not normal cells. The mechanism of action is thought to be due to its ability to coordinate with amines, which may lead to inhibition of amino acid synthesis. 2-Bromopropionyl chloride can also be used as a fluorescence probe for fatty acids, which may be useful for biological studies or clinical response.</p>

<p>4-Bromo-1-butyne is an organic chemical compound that is used as a precursor in the synthesis of pharmaceuticals and agrochemicals. 4-Bromo-1-butyne has been shown to inhibit the growth of T-cell leukemia cells, murine leukemia cells, tuberculosis, and colorectal adenocarcinoma. In addition, 4-Bromo-1-butyne has been shown to be active against bacteria when conjugated with a variety of functional groups such as sulfonamides or amines. The synthetic route for this compound starts from styrene and bromination using NBS followed by 1,4-addition of butyne to the bromide. This process produces a mixture of cis and trans isomers which are separated by chromatography on silica gel.</p>

<p>2,2-Difluoroethyl methyl ether (DEFME) is a nonpolar, hydrophobic compound that can be used as an alternative to isopentane. Radiative data show that DEFME has a higher thermal stability than isopentane, which makes it more suitable for use in high-temperature applications. DEFME has been shown to have synergistic effects with chlorine and amines in the presence of radiation. Furthermore, DEFME can be used to remove chlorinated organic compounds from contaminated water and soil. The chemical properties of DEFME are also ideal for use in polyolefin production and other polymerization processes. The chemical structure of DEFME is similar to that of methylamine and amines, which make it useful as an actuation gas in aerosol cans and other pressurized containers. The atmospheric lifetime of DEFME is long enough that it does not accumulate in the environment or cause environmental pollution when released into the atmosphere.</p>

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<p>Native Melan-A (26-35) decapeptide derives from the melanocyte lineage-specific protein Melan-A/MART-1, which is expressed in almost 75-100% of primary and metastatic melanomas.<br>The region 26-35 of Melan-A protein acts as an antigenic peptide that is recognized by CD8+ tumor-reactive cytolytic T lymphocytes (CTLs) for designing antigen-specific cancer vaccines1. It has been shown that CD8+ Melan-A-specific CTLs isolated from melanoma patients efficiently lyse the Melan-A-expressing HLA-A*0201+ melanoma cell line. However, CTLs preferentially recognize the Melan-A (26-35) peptide as compared with the Melan-A (27-35) peptide. Moreover, the Melan-A (26-35) A27L analog (ELAGIGILTV) has a higher binding affinity to HLA-A*0201 than the native Melan-A (26-35) peptide (EAAGIGILTV), and consequently displays more potent antigenicity and immunogenicity.<br>It has been reported that the concentration of Melan-A (26-35) A27L analog required to obtain 50% of maximal antigenic activity (EC50) is 0.01nM, whereas that of the native Melan-A (26-35) peptide is 0.25nM1. Therefore, the relative activity of Melan-A (26-35) A27L analog is 25 fold higher than that of the native Melan-A (26-35) peptide.<br>Furthermore, functional competition assay has shown that the concentration of Melan-A (26-35) A27L analog required to achieve 50% inhibition (IC50) of tumor lysis is 2nM, which is 10 fold lower than that of the native Melan-A (26-35) peptide. Regarding peptide stability in human serum, the half-lifes (t1/2) of the native Melan-A (26-35) peptide and the A27L analog are quite similar (45 and 40min, respectively) as measured by HPLC-ESI-MS, but much higher than that of the Melan-A (27-35) nonapeptide (5min).</p>

<p>4,5-Dichloro-2-nitroaniline is a chemical compound that has been shown to be an uncoupler of oxidative phosphorylation in ciliates. It is experimentally shown that the reaction yield for 4,5-Dichloro-2-nitroaniline is much higher than that of the corresponding methylbenzene. The two isomers are not detected in the gaseous phase, but only as products of thermal decomposition at high temperatures. Linear regression analysis and predictive models were used to evaluate the transfer and population growth rates at different temperatures. Narcosis was observed in rats exposed to 4,5-Dichloro-2-nitroaniline at concentrations greater than 0.1 ppm (0.1 mg/L).</p>

<p>4-Chloro-2-methoxy-5-methylaniline is a dye molecule that is used in the synthesis of other molecules, such as diketene. It is also used as a solvent, coupling agent, and a dye molecule. This compound can be synthetically prepared by reacting naphthylamine with pyrazolone. The reaction requires catalytic amounts of polyvalent metal salts, such as zinc chloride or iron(III) chloride. The halogenation of 4-chloro-2-methoxy-5-methylaniline to produce 2,4,5-trichlorophenol can be achieved by diazotising the molecule with sodium nitrite and potassium dichromate. 4-Chloro-2-methoxy-5 methylaniline's substituents are methyl groups on the phenyl ring (Cl) and chlorine atoms (C1). Derivatives of this</p>

<p>4-Fluoro-2-nitroaniline is an amide that is a l1210 murine carcinogen. It is also an analytical reagent for the detection of nitrogen atoms in amines and thione compounds. 4-Fluoro-2-nitroaniline has been shown to be effective against cervical cancer, but not cancerous cells, which may be due to its ability to inhibit fatty acid synthesis. The carbon disulphide reacts with the nitro group of 4-fluoro-2-nitroaniline, resulting in the formation of a thione compound.</p>

<p>1-Chloro-2-(chloromethoxy)ethane is an acyclic nucleoside phosphonate that is used as a HIV integrase inhibitor. It binds to the HIV RNA genome and prevents the integration of viral DNA into the host cell's genome, which blocks the replication of HIV. 1-Chloro-2-(chloromethoxy)ethane has been shown to be more potent than other acyclic nucleoside phosphonates in vitro and in vivo. This drug also inhibits herpes simplex virus type 1 (HSV1) thymidine kinase activity, which is essential for viral DNA synthesis. This drug has potential antitumor activities against certain tumor cells due to its ability to inhibit cell proliferation and induce apoptosis through inhibiting rna synthesis.</p>

<p>Please enquire for more information about (S)-1-N-Boc-Propane-1,2-diamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Cesium bromide is a chemical compound that has a high melting point. It is used as an ionic liquid and as a salt in analytical chemistry. Cesium bromide can be used to measure the thermal expansion of materials or to measure the hydrogen bond strength between two molecules. Cesium bromide is also used in membrane systems for water purification, and it can be used for radiation treatment of cancer cells. Cesium bromide can be found in wastewater treatment plants where it helps to remove halides and other contaminants from water vapor, providing kinetic energy to do so. Cesium bromide is also used as an analytical method for measuring hydrochloric acid, uv absorption, or chelate rings.</p>

<p>4-Fluoro(pentafluorosulfanyl)benzene is a fluorinating agent that can be used to produce fluorides, including the trifluoroacetic acid. The cost-effective nature of this compound makes it an attractive alternative to hydrogen fluoride and other fluorinating agents.</p>

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<p>2-Chloro-4-nitro-6-bromoaniline is a dispersive, linear range, ammonolysis and chloride free oxidant for wastewater treatment. This compound is effective at removing organic pollutants from wastewater and has been shown to be both environmentally safe and cost effective. 2-Chloro-4-nitro-6-bromoaniline is also used as a polymerization initiator in the production of polyester resins. It can be manufactured by recycling anilines by reacting them with bromine in the presence of an acid catalyst. 2CNBBA is used as a hydrogen bond acceptor in microextraction of chlorinated compounds from water samples.</p>

<p>Please enquire for more information about 3-Chloro-5-(3-chloropropyl)-10,11-dihydro-5H-dibenz[b,f]azepine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3,4-Diaminobenzotrifluoride is a photophysical agent that emits light of a specific wavelength when irradiated with ultraviolet light. It has been shown to inhibit the growth of human cervical carcinoma cells in vitro and to cause apoptosis in these cells. 3,4-Diaminobenzotrifluoride also inhibits the proliferation of human liver and lung cancer cells in vitro. The mechanism by which this agent causes cell death is unknown. 3,4-Diaminobenzotrifluoride is an acid catalyst and stabilizes the chloride ion. This agent may inhibit DNA synthesis or affect proteins that are involved in signal transduction pathways for cell proliferation.</p>

<p>2,3,7,8-Tetrachlorodibenzofuran (2,3,7,8-TCDF) is a congener of polychlorinated dibenzo-p-dioxin. It is found in the environment as a byproduct from the manufacture of chlorophenols and pentachlorophenol. 2,3,7,8-TCDF is an endocrine disruptor that affects cell nuclei and causes oxidative stress to the liver. There are few studies on 2,3,7,8-TCDF because it is not commercially available for use in research or industry. The only study done on this chemical found that it was potent inducer of glucuronide conjugation enzymes and decreased the activity of rat liver microsomes.</p>

<p>Please enquire for more information about Dichloro(1,1-bis(diphenylphosphino)ferrocene)palladium(II)acetoneadduct including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 2-(4-Methoxyphenyl)-2-(1-hydroxycyclohexyl)ethylamineHydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>9,9-Dichlorofluorene is a bifluorenylidene that reacts with hydrochloric acid to form the trifluoroacetate anion. It is nucleophilic and can be used in organic synthesis to form carbon-fluorine bonds or chloroformates. 9,9-Dichlorofluorene also reacts with chloride ions to form the chloride anion. This reaction yields a high yield and has been used to synthesize other chemicals, including thioacetals and dimethylformamide. 9,9-Dichlorofluorene reacts with protonated nucleophiles in DMF and forms thioacetals following deprotection by hydrochloric acid. The reaction yield of this process is high and it has been extensively studied by NMR spectroscopy.</p>

<p>Cyclobutyl bromide is a cyclopentyl compound that has an hydroxyl group. It is a potent inhibitor of the CB2 receptor, which is primarily expressed on cells of the immune system. Cyclobutyl bromide has been shown to inhibit the uptake of uv light and also has anti-inflammatory properties. Studies have confirmed that this drug inhibits the production of cytokines and chemokines in chronic bronchitis patients, as well as other inflammatory diseases such as rheumatoid arthritis.</p>

<p>Please enquire for more information about 2-Chloro-1-[4-(4-Fluorophenyl)-1-Piperazinyl]Ethanone including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 2-Amino-3,4-dihydro-7-methoxy-2H-1-naphthalenone, hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 21-Amino-17-hydroxypregna-1,4-diene-3,11,20-trioneHydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Oripavine is a naturally occurring alkaloid that can be synthesized from 2,2-bromoethane and potassium carbonate. It has been used for the treatment of Parkinson's disease. Oripavine is an intermediate in the synthesis of rotigotine, a dopamine agonist used to treat Parkinson's disease. The reaction mechanism involves the addition of bromine to 2,2-bromoethane followed by hydrochloric acid treatment to form oripavine. The reaction proceeds with the formation of hydrogen chloride and potassium bromide. The product can then be reacted with a Grignard reagent or allyl group to produce rotigotine.</p>

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Please enquire for more information about (6a,11b,16a)-21-(Acetyloxy)-9-bromo-6-fluoro-11-hydroxy-16-methyl-pregna-1,4-diene-3,20-dione including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>Nonafluoro-5-(trifluoromethyl)cyclohexane is a film-forming polymer that consists of a mixture of long-chain fatty acids, malic acid and sodium citrate. It is used as an intravitreal injection to fill the eye cavity in patients with eye diseases such as macular degeneration or diabetic retinopathy. The polymer is injected into the eye to form a protective layer on the surface of the retina. The film is insoluble and provides an extended release of fatty acids, malic acid and sodium citrate that are then slowly released into the vitreous humor. This decreases inflammation, prevents the formation of new blood vessels, and reduces the risk of neovascularization. Nonafluoro-5-(trifluoromethyl)cyclohexane has been shown to be effective in reducing fat accumulation in animal models with obesity induced by high-fat diets. It also has been shown to limit weight</p>

<p>Calcium bromide is a white solid that has a phase transition temperature of -14.8 °C. It is soluble in water and glycol ether. Calcium bromide can be used to measure the concentration of calcium ions by taking advantage of the high affinity between calcium ions and its salt, calcium bromide, at constant pressure. In this process, water vapor and anhydrous sodium are also adsorbed onto the surface of the solid. The x-ray diffraction data for calcium bromide crystals show that it has a space group of p2 with lattice parameters a = 12.39 Å, c = 10.93 Å, and β = 90°. This salt can be used as a model system for studying reaction mechanisms in chemistry and biochemistry involving ionic liquids or other ionic compounds. The most common application of calcium bromide is as an extractant for volatile organic compounds from air samples using solid phase microextraction (SP</p>

<p>Dichloro(methyl)octadecylsilane is a liquid that is used to coat the inside of tubes in chromatographic columns. The coating ensures that the stationary phase (the material on which the analyte travels) remains stationary and is not carried away with the mobile phase. It has been shown to be effective at removing hydrogen chloride from water and can be used as a fabricating agent for coatings. Dichloro(methyl)octadecylsilane is used in analytical chemistry, where it has been shown to have a number of uses including being able to remove hydroxy groups from molecules and electron microscopy, where it can be used as a coating for nonpolar solvents.</p>

<p>2-Chloro-3-hydroxytoluene is a binder that is used in the treatment of filamentous fungi. It binds to the surface of the filamentous cell and prevents it from growing. 2-Chloro-3-hydroxytoluene has been shown to bind to muscle cells, which may be due to its acidic nature. This chemical also has a disinfectant effect on reticulum cells and muscle fibers.</p>

<p>Please enquire for more information about Deschloro-1,2-dihydro-2-oxo clomiphene HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Chlorodimethyl(3,3,4,4,5,5,6,6,7,7,8,8,8-Tridecafluorooctyl)-Silane is an organic solvent that can be used as a component in the synthesis of synaptic membranes. It has been shown to inhibit spontaneous activity in rat brain slices and exhibits high hydrophobicity. Chlorodimethyl(3,3,4,4,5,5,6,6) - Silane has been used for the patch-clamp technique on human erythrocytes and the immunostaining of proteins. This compound is also useful for the optimization of organic reactions and asymmetric synthesis.</p>

<p>Benzhexol hydrochloride is an ophthalmic, which is used to treat symptoms of eye diseases. It inhibits the immune system and has been shown to be effective in treating autoimmune diseases such as multiple sclerosis. Benzhexol hydrochloride blocks nerve impulses and can cause drooling and hallucinations. This drug can be used in combination with other drugs for the treatment of neurological disorders, including Parkinson's disease. Benzhexol hydrochloride is also used as a diagnostic agent for various conditions, including infectious diseases and geriatric patients with dementia. A linear calibration curve has been observed using a chemiluminescent reaction that is dependent on the concentration-time curve of benzhexol.</p>

<p>Please enquire for more information about [2-(1-Isopropyl-1H-benzimidazol-2-yl)ethyl]amine dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Bromo-2-phenylthiazole is a reactive arylating agent that has been used in the Suzuki reaction to form biaryl compounds. It is also used in the synthesis of heterocycles and alkene cross-coupling reactions. The 4-bromo group can be replaced by other halides, such as chlorides, bromides, or iodides. The substituents on the phenyl ring can be varied to yield different products. Reactive groups are an important factor in optimizing yields and preventing side reactions. This molecule is a useful starting point for the synthesis of complex molecules with functional groups.</p>

<p>Please enquire for more information about (4-Chlorophenyl)methanesulphonyl chloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3,4-Dichlorophenylmagnesium bromide - 0.5M solution in tetrahydrofuran is a chemical reagent that is used to produce methyl compounds. It is often used in the production of chlorinated compounds by substitution of chlorine atoms for hydrogen atoms on the carbon chain. 3,4-Dichlorophenylmagnesium bromide - 0.5M solution in tetrahydrofuran has a molecular structure that includes an electronegative chloro group and a titanium ligand. Acid catalysts are often used with this chemical to promote the reaction between the magnesium and halide ions, which produces methylation products. This may be done through x-ray analysis to determine the progress of the reaction.</p>

<p>B-chlorocatecholborane is a nonpolar solvent that is used in the synthesis of drugs and other organic compounds. It reacts with trifluoromethanesulfonic acid to form a coordination complex, which can be used to synthesize pharmaceuticals. B-chlorocatecholborane can also be used for solid-phase synthesis, which offers an efficient method for chemical reactions. This reagent has been shown to react with 5-hydroxytryptamine 4 (5-ht4) receptor, which is involved in the regulation of appetite and sleep. It also reacts with 2-arachidonoylglycerol (2AG), a lipid molecule that mediates the effects of cannabis on appetite, pain and memory. The structure of this compound was determined using nuclear magnetic resonance spectroscopy and mass spectrometry. The biological properties of B-chlorocatecholborane have not yet been studied.</p>

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<p>Dimethylthiocarbamoyl chloride is an organic compound that can be used to synthesize a hydroxy derivative. Dimethylthiocarbamoyl chloride has been shown to have physiological activities in animal models, including anti-inflammatory activity and oxidative injury. It also has antioxidant properties and can reduce the production of pro-inflammatory mediators such as TNFα, IL-1β, and IL-6. Dimethylthiocarbamoyl chloride is a precursor for the synthesis of many chemical compounds, including drugs and dyes. The hydrochloride salt is commonly used in organic synthesis as a reagent for introducing the methyl group into organic molecules.</p>

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Triarylsulfonium hexafluoroantimonate salts mixed - 50 wt. % in propylene carbonate, also known as TAS-50, is a coating that is used in analytical chemistry and polymerization reactions. TAS-50 has been shown to be biocompatible and non-irritating to skin, eyes, or mucous membranes. It is a fluorescent compound that can be used for the detection of analytes in liquid samples. TAS-50 has been shown to have optical properties that are similar to those of glass. The coating has also been shown to have efficient methods for fabricating optical fibers with improved temperature resistance and radiation resistance.

<p>1,5-Bis(4-allyldimethylammoniumphenyl)pentan-3-one, dibromide is a reversible inhibitor of acetylcholinesterase. It has been shown to inhibit the enzyme activity in vitro and in vivo. 1,5-Bis(4-allyldimethylammoniumphenyl)pentan-3-one, dibromide has been shown to be an effective inhibitor of nicotinic acetylcholine receptors in model organisms such as Xenopus oocytes and Acetylcholine esterase activated rat pheochromocytoma cells. The molecule also inhibits the phosphorylation of pnitrophenyl phosphate by choline kinase. This inhibiting effect on choline kinase leads to a decrease in the concentration of choline available for neurotransmitter synthesis. Monoclonal antibodies against acetylcholinesterase are used to detect this</p>

<p>1-(2-Fluorophenyl)piperazine HCl is a psychoactive drug that belongs to the class of piperazines. The compound has been validated for use in spectra, minimizing, and infrared spectroscopy. The compound has also been shown to be psychoactive and can be used as a screening agent for psychoactive substances. The 1-(2-fluorophenyl)piperazine molecule is approximately linear, with two amide linkages and a phenyl ring at one end. It has a calculated molecular weight of 208 g/mol and an empirical formula of C12H14FN3O.</p>

<p>Cyclopropanecarboxylic acid chloride is an organic compound with a molecular formula of C3H6Cl2O. It belongs to the group of carboxylic acids and has a pyrazole ring, which is a potential drug target. Cyclopropanecarboxylic acid chloride has been found to be active against infectious diseases such as herpes, influenza, and Ebola. The mechanism of action for this compound is not yet fully understood but it has been shown to have an effect on growth factors and kinetic data.</p>

<p>Please enquire for more information about 1-Methyl-2-(piperazin-1-ylcarbonyl)-1H-indole hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(5-Fluoro-2-methyl-1H-inden-3-yl)acetic acid (FMIAA) is a phase transfer catalyst that catalyses the condensation of alkyl esters. It can be used in the condensation of aromatic and aliphatic aldehydes in liquid phase with potassium as a reagent and organic solvent. The FMIAA is then removed by dehydrating the product, leaving it in solid form. FMIAA has been shown to be effective for the synthesis of a wide range of compounds, including pharmaceuticals such as cyclopentanone, aminomethylpiperidine, and 4-aminoquinoline.</p>

<p>Dibenzylfluorescein is a fluorescent probe that can be used for the detection of CYP3A4 enzyme activity. Dibenzylfluorescein has significant cytotoxicity and causes genotoxic effects in human cells, which may be due to its ability to inhibit drug-metabolizing enzymes such as cytochrome P450 (CYP) enzymes. The fluorescence intensity of dibenzylfluorescein is proportional to the amount of CYP3A4 present in the sample. The fluorescence intensity can be quantified using a spectrofluorometer, and the results can be analyzed by high-performance liquid chromatography-mass spectrometry (LC-MS/MS). Dibenzylfluorescein has been used as a marker for CYP3A4 activity in human hepatocyte-like cells and has been shown to have an inhibitory effect on enzyme activities. It also inhibits the</p>

<p>Octafluoro-1,6-hexanediol is a cyclic diol with the chemical formula C6F14O2. The compound is produced by the reaction of hexafluoropropylene oxide and hydrogen fluoride in the presence of a catalyst. This process can be repeated to produce higher molecular weight compounds such as octafluoro-1,8-octanediol (C8F18O2) and octafluoro-1,10-decanediol (C10F22O2). Octafluoro-1,6-hexanediol has been studied using spectroscopies and x-ray crystallography techniques. X-ray crystallographic studies have shown that this molecule has an intramolecular conformation with one hydroxy group on each end of the molecule. Octafluoro-1,6-hexanediol forms crystals that are colorless or light yellow in color. Crystals are monoclin</p>

<p>Please enquire for more information about 4-Fluoro bupropion including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(S)-(+)-Epichlorohydrin is a chlorohydrin that is used as an industrial chemical. It can be synthesized by reacting benzyl chloride with sodium hydroxide in the presence of water. The reaction mechanism for this process involves nucleophilic addition of the chlorine atom to the carbonyl group, followed by protonation and elimination of hydrogen chloride. The stereoselective synthesis of (S)-(+)-epichlorohydrin is based on asymmetric induction by enantiomers of the reactant. This product has been shown to have a constant pressure kinetic study at 0.1 M in acetonitrile and 0.2 M in dichloromethane with a turnover number of 1.4 × 10 mol/L/s, which is comparable to other synthetic methods for epichlorohydrin. Pharmacokinetic data for this product has been shown to show good bioavailability in rats, with a half-life of 0.</p>

<p>4-(Trifluoromethylsulfonyl)benzonitrile is a coupling agent that is used to catalyze cross-coupling reactions between organoboranes and organic electrophiles. It is compatible with a wide range of functional groups, including phosphine and phosphite. 4-(Trifluoromethylsulfonyl)benzonitrile has been shown to be an excellent catalyst for the Suzuki and Miyaura reactions, as well as for arylation reactions. 4-(Trifluoromethylsulfonyl)benzonitrile is not active in the presence of water or oxygen and should be stored in a dry place at room temperature.</p>

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<p>Please enquire for more information about 2-Bromo-3-methylbutenoic acid methyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Chloro-3,5-dimethyl adamantane is a chemical compound that is used as a solvent in the synthesis of other compounds. It is created by hydrolyzing acetonitrile with hydrochloric acid and catalytic reduction with chlorine. This process can be done on an industrial scale, leading to the production of thousands of pounds per day. 1-Chloro-3,5-dimethyl adamantane itself is not toxic to humans or animals, but it has been shown to cause environmental pollution when mixed with salt during the reaction. The use of formamide as a solvent instead of acetonitrile can reduce this risk. !-- --&gt;</p>

<p>Chlorfenvinphos is an organophosphate pesticide that inhibits the enzyme acetylcholinesterase. It is used in agricultural and commercial settings to control insect pests, such as aphids, leafhoppers, and thrips. Chlorfenvinphos has been shown to have acute toxicities in humans and animals, as well as chronic effects on the environment. This chemical has been shown to reduce the activity of enzymes involved in metabolism and cell division. The use of chlorfenvinphos in wastewater treatment systems has been shown to be ineffective at removing this agent from wastewater effluent. Chlorfenvinphos is toxic to aquatic organisms and can cause ecological damage by disrupting the balance of natural ecosystems.</p>

<p>N-(6-Phenylhexyl)-5-chloro-1-naphthalenesulfonamide is a dibutyryl camp analog that has been shown to inhibit the L-type calcium channel in a dose-dependent manner. It has an effect on both spermatozoa and glioma cells, with its most significant effect being inhibition of the intracellular calcium ion. This drug inhibits the growth rate of these cells, which may be due to its ability to activate adrenergic receptors and cause increased intracellular calcium ion levels. N-(6-Phenylhexyl)-5-chloro-1-naphthalenesulfonamide also slows the cycle of the cell, which may be due to a kinetic effect.</p>

<p>3,4-Dichloropropiophenone is an organic solvent that contains a chlorine atom. 3,4-Dichloropropiophenone exhibits significant activity for the removal of chlorinated phenols and other halogenated organic compounds from wastewater. The reaction mechanism of this process involves the conversion of 3,4-dichloropropiophenone to a tetranuclear thiolate complex which then reacts with the halogenated compound to form an imine. This imine is hydrolyzed by hydroxide ion to produce a chlorine-containing product and ammonia. 3,4-Dichloropropiophenone has also been shown to have antimalarial activity.</p>

<p>4-Amino-3-bromoisoquinoline is an isocyanide that reacts with nucleophilic heteroatoms such as the amino group. It also reacts with bromine to form a bromopyridine. The nitrile group of 4-amino-3-bromoisoquinoline can be reduced with sodium borohydride to produce 4-aminoquinoline. This compound has shown potential for use in chemotherapy and treating bacterial infections.</p>

1-Azaspiro[4.4]nonane hydrochloride is a versatile building block that is also used in research, as a reagent, and as a speciality chemical. It has been shown to be an excellent building block for complex compounds, with wide applications in the pharmaceutical industry. 1-Azaspiro[4.4]nonane hydrochloride has a CAS No. of 1417567-64-6 and can be found under the trade name Azapropynalene Hydrochloride (AP). It is soluble in water, alcohols, ethers and acetone but insoluble in most other solvents. 1-Azaspiro[4.4]nonane hydrochloride has been shown to have high quality and stability when stored under appropriate conditions; it is also resistant to degradation by light or air.

<p>Cysteamine 2-chlorotrityl resin is a synthetic polymer that is used in peptidomimetic synthesis. It has been shown to inhibit the growth of cancer cells, and has been studied as a potential therapeutic agent for cancer treatment. Cysteamine 2-chlorotrityl resin has also been studied as an adjuvant for immunotherapy strategies against cancers. Cysteamine 2-chlorotrityl resin interacts with the cell membrane, highlighting its diagnostic and therapeutic potentials.</p>

<p>4-Bromo-pyridine-2-carboxylic acid is a metabotropic glutamate receptor antagonist that inhibits the neurotransmitter glutamate. It has been shown to have antibacterial activity against Staphylococcus aureus and anti-inflammatory properties against the fungus Candida albicans. The drug is orally bioavailable, which means it can be taken by mouth, and has a pharmacokinetic profile that increases its bioavailability. This means that 4-Bromo-pyridine-2-carboxylic acid is an inhibitor of deoxycytidine kinase and may be used as an antifungal agent.</p>

<p>Iloperidone is a white to off-white crystalline powder that is soluble in water and alcohol. It is used as an antipsychotic drug and belongs to the class of benzamides. Iloperidone has been shown to be effective for schizophrenia, bipolar disorder, and major depressive disorder. The chemical name for iloperidone hydrochloride is 4-(2,4-Difluorobenzoyl)piperidine hydrochloride. This drug also has a high affinity for serotonin 5-HT2A receptors in the brain, which may contribute to its therapeutic effects.</p>

<p>Phenylselenenyl bromide is a fatty acid with a selenium atom in the side chain. It has an unsymmetrical structure and reacts with thrombin receptor, leading to the activation of protein C. Phenylselenenyl bromide is also converted to a glucuronide conjugate in the liver. This compound can be used as an immunosuppressant and has been shown to have anti-inflammatory effects in animal models of autoimmune diseases. Phenylselenenyl bromide may also inhibit nitric oxide production by reacting with nitro groups.br&gt; Phenylselenenyl bromide contains nitrogen atoms that are asymmetric because they are not paired together. This means that one of the two nitrogen atoms is surrounded by four different substituents, while the other nitrogen atom is only surrounded by three different substituents. The structure of phenylselenenynl bromide makes it difficult</p>

<p>Please enquire for more information about 2-(3,5-Dichlorophenyl)Pyrrolidine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Bromobenzofuran is a compound that has been shown to have antioxidant properties and can be used for the treatment of chronic kidney disease, hepatitis, and degenerative diseases. It has nitrogen atoms in its structure that are reactive with oxygen, which may cause the release of picolinic acid (PA), a compound that has been shown to have anti-inflammatory properties. 2-Bromobenzofuran is an alkynyl group that binds to receptors such as serotonin and dopamine. This group also has carbonyl groups, which can form adducts with amines. The piperazine ring in 2-bromobenzofuran is activated by reaction with hydroxyl groups.</p>

<p>(E)-5-(2-Bromovinyl)uracil is a drug that has been shown to be effective against leukemic cells. It is a prodrug of 5-bromouracil, which is an antimetabolite and cytotoxic agent. (E)-5-(2-Bromovinyl)uracil has also been shown to be active against solid tumours, such as metastatic colorectal cancer, and bacteria. The mechanism of action involves the irreversible inhibition of the enzyme thymidylate synthase, which catalyzes the conversion of deoxyuridine monophosphate (dUMP) to thymidine monophosphate (dTMP). The drug binds to the dinucleotide phosphate pocket in the enzyme's active site and blocks access by dUMP. This leads to DNA synthesis errors, causing cell death. As a prodrug, it has low toxicity profiles and does not cause bone marrow suppression like</p>

<p>Chloro[2-(di-tert-butylphosphino)-2',4',6'-triisopropyl-1,1'-biphenyl][2-(2-aminoethyl)phenyl)]palladium(II) is a molecule that inhibits the adenosine receptor in autoimmune diseases and cancer. It also has an inhibitory effect on the membrane transport of glucose, glucosan, and aziridine. This drug can be used to treat inflammatory diseases such as diabetes, asthma, and inflammatory bowel disease. The geometric isomers of this molecule are not identical in shape or size and can have different effects on the body.</p>

<p>Chlormequat is a plant growth regulator that is used to inhibit the elongation of roots and shoots. It also inhibits the synthesis of cell wall components, causing cell death. Chlormequat has been shown to have a positive effect on plant growth by increasing water and nutrient uptake. The optimum concentration of chlormequat for plant growth varies depending on the type of plant. It can be determined by measuring the amount of phosphorus pentoxide in tissue culture samples. Chlormequat also blocks signal pathways that are activated by bacterial colony-stimulating factors, inhibiting bacterial growth. The analytical method for determining chlormequat concentrations in plants is based on histological analysis.</p>

<p>Cotarnine chloride is an isoquinoline alkaloid, which is a derivative of the opium alkaloid narcotine. It is synthesized through the oxidation and chlorination of narcotine extracted from opium. The mode of action of cotarnine chloride primarily involves its vasoconstrictive properties, which help in reducing blood flow by contracting smooth muscle fibers in blood vessels. This action aids in achieving hemostasis, thereby preventing or controlling hemorrhage.</p>

<p>3,4-Difluorostyrene is a synthetic compound that can be used to manufacture ticagrelor. It is an organic chemical with the chemical formula C8H6F2O2. 3,4-Difluorostyrene is an organic solvent and can be used as an antithrombotic agent. 3,4-Difluorostyrene has been shown to have optimum temperature of 40°C and is mainly used in preparative reactions.</p>

<p>Dimethylcarbamoyl chloride is a chemical that is used as an ionization reagent in analytical chemistry. It is a colorless liquid with a neutral pH, boiling point of 73 °C, and density of 1.01 g/mL. Dimethylcarbamoyl chloride can be used to synthesize acylated amines and carbonyls for use in pharmaceuticals, polymers, dyes and other chemicals. The chlorine atom can also be substituted with other halogens. The compound has been shown to be chemically stable and resistant to oxidation by catalysts such as oxygen or hydrogen peroxide. Dimethylcarbamoyl chloride is mainly used as an analytical tool for the detection of carbonyl groups in molecules using chemical ionization (CI). Dimethylcarbamoyl chloride has also been shown to have anti-cancer properties due to its effects on choroidal neovascularization (a condition associated with eye diseases) by inhibiting vascular endothelial growth</p>

<p>Please enquire for more information about (S)-5,6,6a,7-Tetrahydro-6-methyl- 4H-dibenzo[de,g]quinoline-10,11-diol hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 7-Bromobenzo[d]oxazole including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Tetrafluoroethane, also known as Freon-12, is a chlorofluorocarbon that has been identified as a potent greenhouse gas. Tetrafluoroethane is a byproduct of the industrial production of fluorochemicals, and its disposal in landfill sites has led to soil contamination. 1,2-Dichloro-2-iodo-1,1,2-trifluoroethane (CIF) is a halogenated hydrocarbon that can be synthesized from tetrafluoroethane using an electrochemical process. CIF is used as a catalyst for telomerization reactions such as the synthesis of polyethylene terephthalate (PET). The efficiency of this reaction increases with higher temperatures and lower potentials. This is due to the increased ionization energy which leads to more efficient electron transfer. The reaction mechanism for the telomerization of furan with ethylene glycol with CIF as catalyst at high</p>

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<p>Please enquire for more information about 2-[(N,N-Dibenzylamino)methyl]cyclohexanone hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Chloro-3-(trifluoromethyl)phenyl isocyanate (4CTFPI) is a phenoxy that has significant antiproliferative activity and can be used to treat cancer. It can inhibit the growth of tumor cells by suppressing the production of growth factors and binding to the receptor for these factors, which leads to inhibition of cell division. 4CTFPI also inhibits tumor growth through its ability to induce apoptosis in cancer cells. 4CTFPI has been shown to have antitumor effects on sarcoma cells in vitro and in vivo with a low toxicity profile. This compound is not active against bacterial infections or fungi, but it does not show any carcinogenic effects.</p>

<p>(Oc-6-21)-(4-Aminophenyl)Pentafluoro-Sulfur is a synthetic chemical that has the molecular formula of CF5SO2NH. It is a five membered heterocycle with an affinity for chloride ions. The compound was synthesized using phenacyl chloride and chlorosulfonyl fluoride in a one step synthesis. This chemical has shown to be an analog of serotonin with hydrogen bonding capabilities. (Oc-6-21)-(4-Aminophenyl)Pentafluoro-Sulfur can act as both a sensor and an electroneutral chlorine ionophore.</p>

<p>O-Chloramine T is a chemical compound that is used in the treatment of cancer. It is an endoreduplication agent and has been shown to cause endothelial cell growth and apoptosis in cancer cells. O-Chloramine T binds to the membrane of cancer cells, which leads to a decrease in autocrine activity and cell binding. O-Chloramine T also inhibits endothelial cell growth by inhibiting protein synthesis and blocking the synthesis of DNA and RNA. This drug has been shown to have anti-cancer properties in animal models and hyperosmolarity properties, which may be due to its ability to cause vessels to collapse.</p>

<p>2-Chloroquinolin-8-ol is a chemical compound that binds to the human serum albumin and has cytotoxic effects on cancer cells. It has been shown to be an inhibitor of survivin, a protein that can promote cancer cell survival. 2-Chloroquinolin-8-ol has also been shown to inhibit the proliferation of human epidermoid carcinoma cells in vitro. This agent also inhibits the growth of Trichophyton mentagrophytes, a fungus that causes tinea versicolor, by binding to the ribosomal RNA. The binding constants for 2-chloroquinolin-8-ol were determined using atomic orbital calculations and vibrational spectroscopy. It has also been shown to bind with high affinity to hepg2 cells and cervical cancer cells.</p>

<p>Myristoyl chloride is an antimicrobial agent that belongs to the group of cationic surfactants. It has been shown to be active against bacteria and fungi, but not against viruses. Myristyl chloride has been used in a number of industries, including food production and processing, for its ability to inhibit microbial growth in acidic environments. This chemical also has anti-inflammatory properties and can be used as a topical treatment for inflammatory diseases such as psoriasis or atopic dermatitis.</p>

<p>1-(3-Fluorobenzyl)piperazine is a potent inhibitor of annexin A1. It has been shown to inhibit the proliferation of pancreatic cancer cells and induce apoptosis in these cells by inhibiting cholinesterase activity. 1-(3-Fluorobenzyl)piperazine also inhibits tumor growth in vivo and induces apoptosis, which may be due to its ability to inhibit the mitochondrial membrane potential. The compound has also been shown to have antitumor effects in other types of cancer cells. This drug is an amine that emits acidic compounds as a result of hydrolysis.</p>

<p>4-(Trifluoromethyl)benzyl amine is a nucleophilic reagent that is used for the asymmetric synthesis of chiral amines. The reaction mechanism involves the nucleophilic attack of the trifluoromethyl group on an electron-deficient carbon atom of a substrate, followed by elimination of hydrogen fluoride. The trifluoromethyl group also acts as a light emitter when irradiated with UV light. 4-(Trifluoromethyl)benzyl amine is able to produce carbonyl groups through irreversible oxidation and has been shown to inhibit cancer cell proliferation in vitro and in vivo. This compound can be found as white crystals and has a polymorphic nature.</p>

[1,2-Bis(diphenylphosphino)ethane]dichloropalladium(II) is a chemical compound that is insoluble in water and soluble in organic solvents. It is a reagent used to prepare other compounds. The synthesis of this compound involves the reaction of chloroform with dichloro[1,2-bis(diphenylphosphino)ethane]palladium (II). The resulting compound has a yellow color due to its ligands, which are amines or halides. This compound can be recrystallized from toluene or ether for use in preparative work. [1,2-Bis(diphenylphosphino)ethane]dichloropalladium(II) has been used as an analytical reagent for the determination of chloride and ligand content in some organic solvents.

<p>S-Ethylisothio urea, hydrobromide is a nitric oxide (NO) synthase inhibitor that prevents the conversion of arginine to NO. It has been shown to inhibit protein synthesis in cells, which may be due to its ability to inhibit guanylate cyclase and intracellular calcium concentrations. S-Ethylisothio urea, hydrobromide has been used in experimental models as an anti-inflammatory drug for the treatment of autoimmune diseases like rheumatoid arthritis. This compound also blocks the production of NO by inhibiting the oxygen transport system in the lungs, which is required for redox potential. S-Ethylisothio urea, hydrobromide is a cyclase inhibitor that prevents the conversion of dehydroascorbic acid to ascorbic acid. It can be used as an antioxidant by scavenging reactive oxygen species and preventing oxidative damage.</p>

<p>2-Chloro-3-ethylbenzoxazolium tetrafluoroborate is a synthetic compound that inhibits the enzyme maltase. This compound is used in the treatment of diabetic patients with intestinal maltase deficiency and has been shown to be effective in clinical studies. 2-Chloro-3-ethylbenzoxazolium tetrafluoroborate has also been shown to inhibit other enzymes, such as thiocarbamate synthetase and aminooxazoline synthetase, which are involved in the biosynthesis of chlorinated pesticides and herbicides. The chloride ion is necessary for this inhibition activity. The compound can be prepared by a preparative method that involves hexaacetate and chloride ion or by using an aglycone, trehalamine, or stereospecific method.</p>

<p>1,2,4-Trichlorobenzene is a chemical compound that has been shown to have chronic oral toxicity in rats. The results of kinetic studies using rat liver microsomes suggest that the enzyme activities of fatty acid synthase and acetyl-CoA carboxylase are inhibited by 1,2,4-trichlorobenzene. This inhibition may be due to the effects of 1,2,4-trichlorobenzene on the activity of these enzymes' cofactors such as adenosine triphosphate (ATP) and nicotinamide adenine dinucleotide phosphate (NADPH). The leaf structure of plants can be altered by 1,2,4-trichlorobenzene. Hydrochloric acid (HCl) is produced when 1,2,4-trichlorobenzene reacts with water and this HCl may result in chain reactions with other chemicals. The surface methodology used</p>

<p>3-Bromo-2-methylbenzoic acid methyl ester is a serotonin transporter and reuptake inhibitor. It has selectivities for serotonin, dopamine and norepinephrine transporters. 3-Bromo-2-methylbenzoic acid methyl ester acts as a linker molecule in the synthesis of complex molecules like neurotransmitters. It is also a bifunctional molecule that can act as an antidepressant or anti-anxiety drug by increasing serotonin levels in the brain. 3-Bromo-2-methylbenzoic acid methyl ester’s function as a ligand is to bind to receptors on cells, which may be linked with its effects on depression and anxiety.</p>

<p>Please enquire for more information about Boc-D-aspartic acid beta-9-fluorenylmethyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>