Organic Halides

<p>1-Iodo-3-(trifluoromethyl)benzene is a reagent used in cross-coupling reactions to form carbon-carbon and carbon-heteroatom bonds. It is soluble in organic solvents, such as benzene and tetrahydrofuran. 1-Iodo-3-(trifluoromethyl)benzene can be used as an organic fluorophore or as an electrophilic halogenating agent. The reaction of 1-iodo-3-(trifluoromethyl)benzene with sodium methoxide yields the corresponding iodonium salt, which has been shown to react with aldehydes, ketones, esters, thiols, and amines to give substituted products. The reaction rate depends on the temperature and the nature of the substrate. 1-Iodo-3-(trifluoromethyl)benzene can also be</p>

<p>Please enquire for more information about Desmethyl fluorometholone 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 N-[3-Fluoro-4-[(methylamino)carbonyl]phenyl]-2-methylalanine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,3-Difluoro pyridine is an organic compound with the chemical formula C6H3F2N. It is a colorless liquid that has a strong odor and a boiling point of 147°C. 2,3-Difluoro pyridine has antibacterial properties and can be used to treat bacterial infections by inhibiting the synthesis of proteins in bacterial cells. This inhibition prevents the formation of new cell walls, which leads to cell death. 2,3-Difluoro pyridine is also used as an intermediate in organic chemistry reactions involving hydrogen fluoride. The transport properties of this compound are low due to its high melting point and low solubility in water. There are three different polymorphs for 2,3-difluoropyridine: form II, form III and form IV, with form II being the most common. Form II has a trigonal planar molecular geometry, whereas forms III and IV have tetragonal</p>

<p>Please enquire for more information about 1,3-Distearoyl-2-chloropropanediol-d5 including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Bromo-6-chloropyridine is a synthetic, nucleophilic bidentate ligand that is used in the synthesis of vismodegib. It inhibits the growth of cancer cells by inhibiting a pathway that regulates cell division and differentiation. 2-Bromo-6-chloropyridine can be used as a cross-coupling agent for the synthesis of other chemicals. This chemical has pharmacokinetic properties and pharmacokinetic properties and can inhibit chloride channels, which may have an inhibitory effect on cancer cells. 2-Bromo-6-chloropyridine is also an effective inhibitor of nucleophilic substitutions, which are involved in many biological processes, such as DNA replication and protein synthesis.</p>

<p>Please enquire for more information about 4-Chloro-3,5-difluorobenzoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,4,4’-Trichlorobiphenyl is a polychlorinated biphenyl congener. It has been shown to have an adverse effect on the central nervous system, causing neurotoxicity. 2,4,4’-Trichlorobiphenyl has been used as a model system for the study of the effects of environmental toxins on mitochondrial membrane potential and lipid peroxidation. 2,4,4’-Trichlorobiphenyl binds to fatty acids in mitochondria and inhibits fatty acid β-oxidation. The inhibition of fatty acid oxidation leads to increased levels of protocatechuic acid in the serum and liver tissue. 2,4,4’-Trichlorobiphenyl has also been found to be toxic to aquatic organisms such as fish and shrimp at low concentrations.</p>

<p>Please enquire for more information about 8-Chloro-6-(2-fluorophenyl)-1-methyl-4H-imidazo[1,5-a][1,4]benzodiazepine 2,5-dioxidemidazolam 2,5-dioxide 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 (+)-(8,8-Dichlorocamphorylsulfonyl)oxaziridine 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 N-Methyl-1-(3,4,5-trimethoxyphenyl)methanamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-(Methylsulfonyl)phenylhydrazine hydrochloride is a sulfone that is used as a radiopharmaceutical agent. It can be used in the diagnosis of Alzheimer's disease and other neurodegenerative diseases. 4-(Methylsulfonyl)phenylhydrazine hydrochloride binds to carbonic anhydrase I and II, which are membrane-bound enzymes that catalyze the reversible hydration of carbon dioxide. This inhibition leads to increased blood pressure and decreased production of platelets, which can lead to thrombocytopenia. The inhibitory potency of 4-(methylsulfonyl)phenylhydrazine hydrochloride on Cox-1 and Cox-2 has been shown to be similar to that of aspirin, but it is more selective for Cox-2.</p>

<p>Clobetasol propionate is an organic acid with a chemical structure that is stable in pharmaceutical preparations. It is used to treat inflammatory skin disorders such as psoriasis and atopic dermatitis. Clobetasol propionate is an impurity of clobetasol, which has been shown to be chemically stable in preparations. The clobetasol propionate compound has been found to be more potent than other topical corticosteroids for the treatment of plaque psoriasis and atopic dermatitis.</p>

<p>Please enquire for more information about (S)-1,2,3,4-Tetrahydro-5-methoxy-N-propyl-2-naphthalenamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Bromo-4-nitrobenzene is a bromonitrile that is used to synthesize optical sensors. It is an intermediate in the synthesis of 1,5-dibromo-4-nitrobenzane, which was used as a model system for the reaction mechanism of coupling reactions. The coupling of 1-bromo-4-nitrobenzane with hydrochloric acid and palladium catalysts leads to the formation of a diazonium salt. This reaction can be analyzed by looking at the nitro group and the halides in the molecule. The nitro group reacts with ammonia to form an aminonitrile and water. Halides react with ammonia to form ammonium salts and hydrogen halides. Diazonium salts are then generated by adding nitrous acid (HNO2) or hydroxylamine (NHOH) to these compounds. Finally, transfer reactions are carried out by heating 1</p>

<p>(2S,3S)-5-[2-(Dimethylamino)ethyl]-3-hydroxy-2-(4-methoxyphenyl)-2,3-dihydro-1,5-benzothiazepin-4-one hydrochloride is a racemic mixture of two enantiomers. It is a prodrug that is hydrolyzed to its active form, diltiazem. The drug has been shown to be effective in the treatment of hypertension and angina pectoris. (2S,3S)-5-[2-(Dimethylamino)ethyl]-3-hydroxy-2-(4-methoxyphenyl)-2,3-dihydro-1,5-benzothiazepin-4-one hydrochloride has been shown to inhibit the activity of the enzyme phosphodiesterase which breaks down cyclic AMP. This inhibition results in an increase in levels of</p>

<p>Dichloromethylsilane (DCS) is a chemical compound that is used in the synthesis of silicone rubber, silicone elastomers, and silicone sealants. It can also be used as a cross-linking agent for polymers such as polyurethane, epoxy resin, and silicone. The synthesis of DCS is achieved by reacting chlorosilanes with methyl alcohol or methyl chloride in the presence of an acid catalyst. DCS exhibits high chemical stability and can be activated at room temperature. This product has been shown to be useful for fabricating medical devices that are implanted into the human body because it does not react with water or blood.</p>

<p>Please enquire for more information about 2-(Fluoromethyl)-3-(2-methylphenyl)-6-nitro-3H-quinazolin-4-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Terephthalaldehyde chloride is a water-insoluble, white solid that is soluble in organic solvents. It forms a protective layer on metal surfaces and plastics, preventing corrosion and microbial growth. Terephthalaldehyde chloride has been shown to be effective against Escherichia coli, Klebsiella pneumoniae, Bacillus subtilis, Pseudomonas aeruginosa, Staphylococcus aureus, and Salmonella enterica. Terephthalaldehyde chloride's antimicrobial activity is attributed to its acid complex with phosphorus pentoxide and electrochemical impedance spectroscopy data indicate that it reacts with the anionic sites of bacterial cell walls. Terephthalaldehyde chloride does not react with human serum proteins or ester linkages; however, it has toxic effects on mice at high doses.</p>

<p>2,4-Dibromobutyryl chloride is an enantiopure compound that can be used as a chemical building block in the synthesis of many other chemical compounds. It has been shown to have butyric acid mediated effects on diabetes and the condition of the esters. 2,4-Dibromobutyryl chloride has also been shown to have stereoselective effects on glucokinase and ketones.</p>

<p>Please enquire for more information about 3-(6-Chloro-1-isopropyl-1H-benzimidazol-2-yl)propanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Oxo Rosuvastatin is a drug product that has been synthesized from natural ingredients. It is an analytical standard for the impurity, 5-oxo-rosuvastatin, which is a potential impurity in the API, rosuvastatin. This drug product has been custom synthesized in order to provide an Impurity Standard for HPLC. This drug product is also used as a Synthetic Reference Standard for Drug Development and Research and Development.</p>

<p>2-Bromobenzo[d]thiazol-6-ol is a diagnostic agent that is used in positron emission tomography (PET) scans to detect Alzheimer's disease. 2-Bromobenzo[d]thiazol-6-ol binds to amyloid plaques and deposits of beta amyloid peptide, the hallmark of Alzheimer's disease. It can be synthesized by cross coupling nitro compounds with aminoacids or by alkylation of nitro compounds with alkenes. Other methods for its synthesis include the microwave irradiation of bromobenzene and thiourea in a nitric acid medium. This compound undergoes metabolism via cytochrome P450 enzymes to form benzo[d]thiazole-2,6(3H)-diol, which is then oxidized by NADPH to form benzo[e]thiazole-2,6(3H)-quinone.</p>

<p>Dechlorane 603 is a polychlorinated biphenyl (PCB) that has chlorine atoms in the 2, 3, and 4 positions. It is produced as an unintentional byproduct of the production of polychlorinated biphenyls (PCBs). The analytical method for Dechlorane 603 is gel permeation chromatography. It can be found in human populations with higher levels in infants than adults. Levels have been shown to be lower in those who eat more fish or who have a high fat diet. Dechlorane 603 levels are higher in pregnant women than non-pregnant women. Animal experiments have shown that it can impair development of the brain and reproductive organs.</p>

<p>Ternary mixtures of hexadecafluoro(1,3-dimethylcyclohexane) with fluorine and hydrogen fluoride are stable compounds. The proton is a constant, which is the only variable in the equation. The analytical method for determining the amount of hexadecafluoro(1,3-dimethylcyclohexane) in a mixture can be found in reference 1. This reference also discusses the matrix effect on this compound's stability and optical properties. Reference 2 discusses transfer reactions that are present when hexadecafluoro(1,3-dimethylcyclohexane) is heated to temperatures of 400°C or above. Reference 3 discusses how polymer films can be formed by heating hexadecafluoro(1,3-dimethylcyclohexane) with a solvent such as pentane. Reference 4 discusses how covid-19 pandemic has been shown to be effective against the H2 strain of subt</p>

<p>Please enquire for more information about 2-Iodo-5-methylpyrimidine 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 L-Glutamic acid gamma-tert-butyl ester alpha-amide hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>[2-(4-Chlorophenyl)-1,3-thiazol-4-yl]acetic acid is a potent antimicrobial agent that inhibits the growth of bacteria by binding to the 50S ribosomal subunit. It has shown antiinflammatory properties in animal models of bowel disease, skin cancer, and autoimmune diseases. This drug has also been shown to have no observable toxicity in humans at doses up to 5000 mg/day for 28 days. The drug binds to a number of enzymes including reactive oxygen species (ROS) scavengers and metabolic enzymes. There are no known drug interactions with this drug and it can be used safely with other nonsteroidal antiinflammatory drugs (NSAIDs).</p>

<p>Cyclopropanesulfonyl chloride (CPSC) is a bicyclic heterocycle that has been shown to have potent inhibitory activity against the human pathogens hepatitis B virus, dengue virus, and influenza A virus. CPSC inhibits the NS3 protease of these viruses by forming hydrogen bonding interactions with the nucleophilic nitrogen atom of the enzyme and also by competing with a chloride ion for binding to the chlorine atom on the enzyme. It also inhibits HIV-1 infection in cell culture experiments. CPSC has been found to be effective in preventing inflammation caused by cytokines, such as interleukin-1β, tumor necrosis factor-α, and prostaglandin E2. The inhibition of inflammatory cytokines may be due to its ability to bind glucocorticoid receptors.</p>

<p>Sodium N-(6-chloropyridazin-3-yl)sulphanilamidate (NPS) is a sulfa drug that has been shown to have an effect on the enzyme activities of some endoparasites, such as Giardia lamblia and Entamoeba histolytica. The active form of NPS is metabolized through a number of metabolic transformations, including hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or conjugation with glucuronic acid. It also specifically binds to markers expressed at high levels in Mycobacterium tuberculosis strains (e.g., ESX-1 secretion system protein) and inhibits cell growth in culture.</p>

<p>7-Chloro-2-hydrazino-5-phenyl-3H-1,4-benzodiazepine is a metabolically stable benzodiazepine that binds to the benzodiazepine receptor. It has been shown to have a higher affinity for this receptor than alprazolam and other related compounds. 7-Chloro-2-hydrazino-5-phenyl-3H-1,4-benzodiazepine has been used as an active ingredient in a number of pesticide products that are used against termites and ants. This compound has also been found to be an effective insecticide against mosquitoes. 7C2HDBZ has been shown to be stable in the environment and is not readily degraded by hydrolysis or pyrolysis.</p>

<p>Please enquire for more information about N-[4-Amino-3-(trifluoromethyl)phenyl]-2-methylpropanamide 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-(Chloromethyl)-3-(2-methoxyphenyl)quinazolin-4(3H)-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Butropium bromide is a biocompatible polymer that is used as an occlusive dressing for wounds. It is made of polyethylene and silicone elastomer, which are both highly resistant to water vapor and reactive chemicals. Butropium bromide has been shown to have high resistance against radiation, allergic reactions, and leukocyte antigen. The particle size of butropium bromide ranges from 0.3-0.5 microns in diameter; the material is soft and flexible with an elastic recoil.</p>

<p>N-Acetyl-S-(1,2-dichloroethenyl)-L-cysteine is a reactive compound that is formed from the metabolism of acetaminophen. It has been shown to cause oxidative injury in the mitochondria of proximal tubule cells. N-Acetyl-S-(1,2-dichloroethenyl)-L-cysteine disrupts mitochondrial membrane potential and causes ATP depletion. It also causes mitochondrial dysfunction by inhibiting respiratory chain activity and lowering cytosolic calcium levels. N-Acetyl-S-(1,2-dichloroethenyl)-L-cysteine has been shown to be toxic in animals and humans. The main analytical method used to detect this compound is the tetrazolium dye assay.</p>

<p>Bis(pyridine)iodonium tetrafluoroborate is a reagent that can be used to iodinate organic compounds. It is prepared by the reaction of pyridine with iodine and bromine in tetrafluoroboric acid. Bis(pyridine)iodonium tetrafluoroborate is an active compound that can be used for amino acid analysis, optical properties, and functional groups. This compound also can be used for magnetic resonance analysis, palladium-catalyzed coupling, and synthetic reactions. Bis(pyridine)iodonium tetrafluoroborate has been found to have radiation transport properties and a strong reactivity towards acids.</p>

<p>2-Bromo-3-nitrobenzoic acid is a reactive chemical used as an antibacterial agent. It inhibits the growth of staphylococcus by inhibiting the synthesis of DNA and protein, which are required for cell division. 2-Bromo-3-nitrobenzoic acid is also effective against mammalian cells, but not against bacteria that grow in a thionyl environment. The chemical reacts with chloride to form 2-bromo-3-chlorobenzoic acid, which can be converted to mercaptoacetic acid by means of reduction with sodium dithionite. Mercaptoacetic acid inhibits bacterial growth by blocking the synthesis of proteins necessary for cell division. 2-Bromo-3-nitrobenzoic acid is synthesized from bromine and nitric acid, while mercaptoacetic acid is synthesized from bromine and acetic anhydride.</p>

<p>trans-Heptachlor epoxide is a pesticide that is used in agriculture and industry. It can be detected by various analytical methods, including mass spectrometry. The chemical structure of trans-heptachlor epoxide has been determined by mass spectrometric analysis. This compound has been found to exist as two stereoisomers, with the cis form being more stable than the trans form at ambient conditions. Magnetic resonance spectroscopy has been used to study the rotational motion of the hydrocarbon chain. Validation of analytical methods for this compound is necessary due to its limited availability and high reactivity with other compounds in the environment.</p>

<p>4'-Chloroacetophenone is a chemical substance that is used in the synthesis of other substances. It has been shown to be an effective tool for cell-specific reactions, such as methyl ketones and benzaldehyde. 4'-Chloroacetophenone reacts with hydrochloric acid and palladium complexes to produce electron reduction, which leads to the activation of methyl ketones. This reaction provides a method for synthesizing molecules with a carbonyl group. The isolated yield of this reaction is dependent on the reaction solution temperature and concentration. The mechanism of this reaction appears to be Suzuki coupling reaction.</p>

<p>Please enquire for more information about H-Leucinol-2-chlorotrityl resin including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Adiphenine hydrochloride is a hydrogen-bonded molecule that is soluble in water. This drug has been used as an occlusive agent in the management of cervical cancer and synchronous fluorescence diagnosis. Adiphenine hydrochloride exhibits thermodynamic data that can be used to calculate its solubility, vapor pressure, and log octanol-water partition coefficient (log Kow). It can also be used as a fluorescent probe for diagnosing cancer by measuring the fluorescence resonance of adiponitrile.</p>

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

<p>L-Methionine tert-butyl ester hydrochloride is a peptide that is used for the treatment of lysosomal storage diseases. It is a metabolic precursor for polypeptides and may be useful for the treatment of tissue damage due to elimination. L-Methionine tert-butyl ester hydrochloride has been shown to have a stable half-life in murine studies, and it is eliminated primarily by the kidneys. Radiometabolites with short half-lives are found in blood and urine samples following intravenous administration. The elimination rate of L-Methionine tert-butyl ester hydrochloride can be calculated by measuring the radioactivity in urine over time.</p>

<p>Please enquire for more information about 2-Amino-5-nitroindan 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 1-Benzyl-4-bromo-3,5-dimethyl-1H-pyrazole 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 N-Methylcarbonyl-2-chloroacetamidrazone including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Bis(2,2,2-trifluoroethyl)amine is a colorless liquid that is soluble in water. It has a molecular weight of 122.11 and a boiling point of 217°C. Bis(2,2,2-trifluoroethyl)amine reacts with tetramethylammonium to form a dimer. The reaction is reversible and the bis(2,2,2-trifluoroethyl)amine can be regenerated by the addition of fluoride or an acid such as hydrochloric acid or sulfuric acid. Bis(2,2,2-trifluoroethyl)amine has an anion that can accept a proton from another molecule. This anion is also known as the bisulfite ion which reacts with hydrogen peroxide to form bisulfate and water.</p>

<p>Tetrafluoroterephthalonitrile is a hydroxyl group-containing organic chemical compound with the molecular formula (CF)CO. It has been used in analytical chemistry as a reagent for the determination of peptide binding constants and disulfide bonds. Tetrafluoroterephthalonitrile binds to nucleophilic sites on proteins, such as the pim-1 protein, and can be used to transport other molecules across cell membranes. In addition, it has been used to produce polymers for use in analytical chemistry. This chemical is also able to bind with magnetic particles under constant pressure conditions, which makes it useful for optical sensor applications. Tetrafluoroterephthalonitrile is a hydroxyl group-containing organic chemical compound with the molecular formula (CF)CO. It has been used in analytical chemistry as a reagent for the determination of peptide binding constants and disulfide bonds. Tetrafluoroterephthal</p>

<p>3-(Trifluoromethyl)benzyl chloride is a chloromethylating agent that reacts with magnesium to form a magnesium chloride solution. 3-(Trifluoromethyl)benzyl chloride is also used in the synthesis of pharmaceuticals, pesticides, and dyes. The reaction produces small amounts of chlorinated byproducts such as chloride, which can be found in wastewater. This chemical has been shown to have adverse effects on the environment through its release into waterways or the atmosphere.</p>

<p>Please enquire for more information about Bromoacetic acid-13C2 including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Chloro-4'-hydroxybenzophenone is a chemical intermediate that is used to produce p-hydroxybenzoic acid by acylation reaction with hydrochloric acid. The optimal reaction of 4-chloro-4'-hydroxybenzophenone with hydrochloric acid occurs at a temperature of 40 degrees Celsius and an excess of 2 equivalents of hydrochloric acid per equivalent of 4-chloro-4'-hydroxybenzophenone. This chemical intermediate has been shown to be an environmental pollutant, as it reacts in the atmosphere with ozone or other oxidizing agents to form hydrogen chloride and aluminium chloride. The transfer mechanism for this process is not yet well understood, but it may be due to demethylation followed by chlorination.</p>

<p>Please enquire for more information about (7-bromo-2H-1,3-benzodioxol-5-yl)methanol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Cobalt chloride is the inorganic compound with the chemical formula CoCl2.6H2O. It is a salt of cobalt in the form of a hexahydrate, which means that it contains six water molecules per molecule of cobalt. Cobalt chloride can be used as a chelate ligand to bind metal ions and prevent them from reacting with other substances. In this way, it can be used in wastewater treatment to remove heavy metals such as copper and zinc, or to remove nitrogen from waste water. The cobalt ion binds reversibly to two oxygen atoms on each molecule of hydrogen peroxide, forming HCoO3HO. This process converts one mole of hydrogen peroxide into one mole of water vapor and one mole of oxygen gas. It also catalyzes reactions involving organic compounds containing ammonia, such as ammonium salts or urea-ammonia solutions - reactions that are used for industrial purposes or for agricultural fertilizers. Cobalt chloride hexahydrate has</p>

<p>Phenyl trifluoromethylsulfide is a diazonium salt that reacts with serine proteases to form reactive functional groups, resulting in the formation of reaction products. The chlorine atom in phenyl trifluoromethylsulfide reacts with hydroxide ions, forming a chloroformate anion. This anion then reacts with nucleophilic amino acids such as lysine and arginine in the protease. This nucleophilic attack induces inflammation in inflammatory diseases such as asthma and arthritis. Phenyl trifluoromethylsulfide has been shown to be effective against ns3 protease found in plasma mass spectrometry samples of patients with chronic respiratory disease (COPD).</p>

<p>N,N,N-Tributyl-1-Butanaminium 1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluoro-1-octanesulfonate is an organic solvent that belongs to the group of surfactants. It is used as a crosslinking agent and ionizing agent in uncured coatings. This chemical has shown proton conductivity and the ability to generate hydroxyl ions when exposed to radiation such as ultraviolet light or gamma rays. NBDBS has been shown to be an effective antigen for use in immunological assays.</p>

<p>1-(4-Fluorobenzyl)piperazine is a potent tyrosinase inhibitor and has been shown to inhibit the proliferation of human cancer cells. It has been found to have inhibitory activity against the amine oxidase enzyme, which is involved in the biosynthesis of pro-inflammatory cytokines. The biochemical properties of 1-(4-fluorobenzyl)piperazine have been studied by liquid chromatography and mass spectrometry and it has been found to be synthesized from piperazine and an amine. There are no other studies available on this drug at this time.</p>

<p>Please enquire for more information about 7-Chloro-5-(2-fluorophenyl)-2-methylamino-3H-1,4-benzodiazepine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Bromo-2-(4-bromophenyl)-2,2'-dimethylacetic acid (2bpd) is the sodium salt of 2-(4-bromophenyl)-2,2'-dimethylacetic acid. It is a metabolite of terfenadine and thionyl chloride. 2bpd has been shown to be an inhibitor of the histamine H1 receptor. This drug is also a brominated derivative of 2-amino-2-methyl-1-propanol, which has been shown to be an inhibitor of the histamine H1 receptor.</p>

<p>2'-Chloro-2-bromoacetophenone is a compound that belongs to the class of methyl ketones. It is known to have a high transfer hydrogenation activity and has been used in the synthesis of phenacyl, which is an important biomolecular. It also has a low toxicity and does not irritate skin or mucous membranes. 2'-Chloro-2-bromoacetophenone can be used as an antiarrhythmic agent for respiratory disorders. This compound can be used for formylation reactions, such as those found in microbial metabolism, due to its ability to transfer hydrogen from organic compounds.</p>

<p>Please enquire for more information about 5-({[2-(4-Chlorophenyl)-1,3-oxazol-4-yl]methyl}thio)-1,3,4-thiadiazol-2-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Silver trifluoromethanesulfonate (AgOTf) is a precursor in the synthesis of alpha-bromo-m-tolunitrile. It is a colorless, odorless solid that can be prepared by the reaction of silver ions with bromine and toluene in an aqueous medium. The profile of AgOTf has been studied by titration method and it has been shown to have an oxadiazole group. This molecule also has anticancer activity against cancer cells. Alpha-Bromo-m-tolunitrile is currently being investigated for its potential use as a drug candidate for the treatment of cancer, with particular interest in the inhibition of angiogenesis and metastasis.</p>

<p>Diisopropylammonium dichloroacetate (DADCA) is a chemical that inhibits the metabolism of glucose. It has been shown to have a hypoglycemic effect in rats and is being investigated as a treatment for metabolic disorders such as diabetes and obesity. DADCA has also been shown to reduce liver lesions in animals with chronic viral hepatitis, and has been found to be effective in reducing tumor growth in mice. This drug can also be used to treat bowel disease by reducing the amount of ammonia released by bacteria. DADCA may also have physiological effects on humans, including an increase in blood pressure and fever, although these effects have not yet been studied.</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>

<p>Phenyl chloroformate is a phenyl compound that is used as a reagent for cationic polymerization. This chemical reacts with amines to form an N-substituted amide in the presence of hydrogen chloride. The mechanism of this reaction is based on nucleophilic substitutions by the hydroxyl group of the phenyl group. Phenyl chloroformate has been used in the synthesis of fatty acids, which are important components of metabolic disorders such as diabetes mellitus type 2.</p>

<p>2,6-Dichlorophenylacetic acid is an inhibitor of the enzyme acetylcholinesterase. It has been shown to be effective in a number of functional assays and is efficient at inhibiting the uptake of 2,6-dichlorobenzoic acid in cells. The inhibition of this enzyme by 2,6-dichlorophenylacetic acid may be due to its protonation and binding to the active site. This binding prevents the release of the acetylcholine molecule that has been bound to the enzyme's active site. This results in increased levels of acetylcholine in the synaptic cleft, leading to an increase in neurotransmitter activity, which can have a variety of effects on neuronal function. 2,6-Dichlorophenylacetic acid also inhibits cell proliferation and induces apoptosis (programmed cell death) in Caco-2 cells by inhibiting protein synthesis.</p>

<p>Diisopropyl(bromomethyl)boronate is a reagent used in organic synthesis. It is an alkynyl boronic ester that reacts with alkenes to form new carbon-carbon bonds. Diisopropyl(bromomethyl)boronate can be used for the asymmetric synthesis of α,β-unsaturated carbonyl compounds and other oxidations of aldehydes and ketones. This reagent has been shown to have a high yield, solvents are not required for its preparation, and it is stable at room temperature. Diisopropyl(bromomethyl)boronate also reacts with haloalkanes and argon gas to generate organoboranes.</p>

<p>Pinaverium bromide is a drug with anti-inflammatory properties. It is used in the treatment of bowel disease and as a muscle relaxant. Pinaverium bromide has shown efficacy in treating bowel syndrome, but it also reduces blood flow to the bowel. Pinaverium bromide inhibits voltage-dependent calcium channels, leading to muscle relaxation. This drug also has been shown to inhibit the production of inflammatory mediators such as prostaglandins and leukotrienes, which may be due to its ability to inhibit basic fibroblast growth factor production. Pinaverium bromide is an effective drug that is used for the treatment of bowel disease and muscle spasms. It blocks voltage-dependent calcium channels, which leads to muscle relaxation without affecting heart function. The inhibition of basic fibroblast growth factor production may contribute to this drug's anti-inflammatory effects.!-- START: Description --&gt; Pinaverium bromide</p>

<p>Dibenzylamine is a tertiary amine with the chemical formula C6H12N2. Dibenzylamine is a colorless liquid that boils at 110°C and freezes at -50°C. It has a density of 0.859 g/mL and a refractive index of 1.539. When heated, it decomposes to form dipropylamine, dibutylamine, and dicyclohexylamine. It also reacts with nitric acid to form an explosive compound called nitrobenzene or dinitrobenzene. Dipropylamine is a colorless volatile liquid that has the chemical formula C6H12N2 and boils at 130°C. When heated, it decomposes to form dibutylamine and dicyclohexylamine. Dibutylamine is a colorless volatile liquid that has the chemical formula C6</p>

<p>Please enquire for more information about 2,4-Dibromo-1-methyl-1H-imidazole including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>L-Serine amide hydrochloride is a synthetic, anti-HIV drug that is used as an antiviral agent. It inhibits the viral life cycle by inhibiting the activity of acyclic nucleoside phosphonates, which are vital to viral DNA synthesis. L-Serine amide hydrochloride binds to the cyclopentane ring of guanosine and prevents its interaction with the enzyme ribonucleotide reductase. This binding prevents the conversion of guanosine into GTP, thereby preventing HIV from using this molecule in their life cycle. L-Serine amide hydrochloride is not active against cellular proteins or prostaglandins.</p>

<p>Please enquire for more information about 2-Amino-3',4'-dimethoxypropiophenone 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 3,5-Dibromo-6-methylpyrazin-2-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Chloro-1H-imidazo[4,5-b]pyridin-2(3H)-one is a chemical compound that is used in analytical chemistry as an insecticide. It has been shown to cause genotoxic activity in weevils exposed to light. The compound has also been shown to have long term efficacy in plants and toxicity studies on animals. 5-Chloro-1H-imidazo[4,5-b]pyridin-2(3H)-one is metabolized by detoxification enzymes and excreted through the urine.</p>

<p>Phenylpropylmethylamine hydrochloride is a chemical compound with the molecular formula CHClN. It is soluble in water and organic solvents. Phenylpropylmethylamine hydrochloride can be prepared by reacting chloropropane with hydrogen chloride, or by reacting phenylpropanolamine with hydrochloric acid in the presence of dodecyl mercaptan and sodium hydroxide solution. The impurities present in this product include chloropropane, chloride gas, and hydroxide ions. The reactions involved are exothermic reactions that require cooling to prevent overheating. Impurities may also form if this product is not reacted under an inert atmosphere of nitrogen gas.<br>The following are some common uses for Phenylpropylmethylamine hydrochloride:<br>-as a solvent in the production of certain types of plastics<br>-in the manufacture of dyes, drugs, rubber products, and soaps<br>-in research</p>

<p>Stannous chloride anhydrous is a particle with a particle size of 3-6 microns and a melting point of 8°C. It has been shown in toxicity studies to be non-toxic to rats and rabbits when administered orally. Stannous chloride anhydrous is a coordination compound that contains stannous ion, which is coordinated by four sulfur atoms and two nitrogen atoms. The molecule can also have different geometries depending on the solvent used; for example, in trifluoroacetic acid, it adopts a trigonal bipyramidal geometry. Stannous chloride anhydrous has been shown to inhibit enzymes such as pepsin, chymotrypsin, and trypsin. This inhibition may be due to its ability to bind covalently with these enzymes.</p>

<p>N-Ethylhydroxylamine hydrochloride is a chemical compound that belongs to the group of biocides. It is used as an antimicrobial agent in medical devices, such as catheters and dialysis membranes. N-Ethylhydroxylamine hydrochloride is also used in cancer research to activate the CCR5 receptor, which is involved in HIV infection. N-Ethylhydroxylamine hydrochloride has been shown to have biological properties in humans and animals and has a high degree of chemical stability. The compound can be synthesized from sodium carbonate and ethyl alcohol. The synthesis involves the addition of ethylene oxide to ethanolamine followed by hydrogenation with a catalyst. N-Ethylhydroxylamine hydrochloride is soluble in water, methanol, and acetone. This chemical compound binds to proteins in the human body, resulting in an increase of acidity in urine samples when tested using a plate test. It also has</p>

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

<p>Kisspeptin-54 is a mammalian peptide hormone that regulates the release of gonadotropin-releasing hormone (GnRH) from the hypothalamus. Kisspeptin-54 has been shown to be potently immunogenic in humans and can be used as an antigen for the production of monoclonal antibodies. It is also a candidate drug for the treatment of obesity and may have neuroprotective effects. Kisspeptin-54 has been shown to reduce body mass index, which may be due to its ability to stimulate the immune system and promote antibody production against tumors. This peptide also has potent on-line binding properties that are useful in polymerase chain reactions.</p>

<p>Please enquire for more information about (1S,3S)-Methyl 3-aminocyclobutane carboxylate hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Dichloro(1,5-cyclooctadiene)palladium(II) is a stable metal complex in which the chlorine atom is coordinated to two benzyl groups and one palladium atom. The chloride ion is coordinated to the palladium atom through a strong coordinate bond. The chloride ion is also coordinated to the two benzyl groups by weaker coordinate bonds. In the presence of sodium carbonate, hydrogen chloride and nitrogen gas, dichloro(1,5-cyclooctadiene)palladium(II) reacts with hydrogen chloride to form stable complexes that are soluble in water. These complexes can be used as catalysts for organic reactions because they are able to transfer hydrogen atoms between molecules without breaking covalent bonds. Dichloro(1,5-cyclooctadiene)palladium(II) has been shown to have antibacterial activity against Staphylococcus aureus and Pseudomonas aeruginosa</p>

<p>3-Bromo-5-fluoropyridine is a synthetic dyestuff that is used in the production of dyes and pigments. It has an analogous structure to 3-amino-5-bromopyridine, which is used as a medicine for treating epilepsy. 3-Bromo-5-fluoropyridine reacts with acetoacetate or ethyl acetoacetate to form methylated products, such as 3-(4'-hydroxyphenyl)propionate. This compound can be synthesized by halogenation with bromine or chlorination followed by hydrolysis. The synthesis of 3-bromo-5-fluoropyridine from 3-amino-5-bromopyridine involves a series of reactions, including diazonium salt formation, followed by bromination and reduction to produce the desired product.</p>

<p>(2,4-Dichlorophenoxy)acetic acid sodium salt monohydrate is a chemical that belongs to the phenoxy herbicides. It is used as a selective herbicide for control of annual and perennial grasses and broadleaf weeds in noncrop areas. This compound has been detected by gas chromatography/mass spectrometric analysis after a dispersive solid-phase extraction procedure. The target analytes were found to be acidic with an unknown molecular weight.</p>

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

<p>3-Aminophenylsulphur pentafluoride is a synthetic chemical compound. It is a ligand with an electron-withdrawing group and has been shown to be a strong oxidizing agent. 3-Aminophenylsulphur pentafluoride reacts with phosphine oxides, yielding phosphines. This reaction can be used for the synthesis of heterocycles that contain phosphorus in their ring system. 3-Aminophenylsulphur pentafluoride also reacts with alkyl halides to produce heterocycles containing sulphur, such as pyridines or thiophenes. The reaction time between 3-aminophenylsulphur pentafluoride and alkyl halides is dependent on the oxidation potential of the alkyl halides, which can be determined by measuring the absorption spectra of the resulting heterocycles. 3-Aminophenylsulf</p>

<p>Bromoferrocene is a ligand that binds to the ferrocenecarboxylic acid skeleton. It is an aromatic hydrocarbon that has been shown to be a potent inhibitor of cervical cancer proliferation. Bromoferrocene was synthesized by a Friedel-Crafts reaction between styrene and hydrobromic acid. The bromine atom in this compound is electron-withdrawing and therefore has radical character, which makes it a reactive molecule with potential for biological activity. Bromoferrocene is chiral and thus can exist as two enantiomers - one with R configuration, the other L.</p>

<p>RU 58841 is a non-steroidal anti-androgen, which is a chemical compound sourced through synthetic processes in pharmaceutical laboratories. It functions by selectively binding to androgen receptors in the hair follicles, thereby inhibiting the action of androgens such as dihydrotestosterone (DHT). This mode of action prevents DHT from activating the receptor, which is a critical factor in the miniaturization of hair follicles.</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 1-(4-Chloro-3-Trifluoromethylphenyl)Piperazine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Lithium difluoro(oxalato)borate is an electron-microscopic corrosion inhibitor that belongs to the class of ester compounds. It is a solid compound that has been shown to be efficacious against oxidation products. The efficiency of this compound is dependent on the concentration and purity of lithium difluoro(oxalato)borate and the type of metal, such as steel or aluminum. Lithium difluoro(oxalato)borate can be used in rechargeable batteries, due to its transport properties, high salt tolerance, and low self-discharge rate. This compound has been shown to have functional groups that are capable of interacting with hydrogen fluoride in an organic solution.</p>

<p>Adrenalone hydrochloride is a synthetic form of epinephrine, which is an endogenous catecholamine. Adrenalone hydrochloride has been used to treat autoimmune diseases and bowel disease. Adrenalone hydrochloride binds to the alpha and beta receptors on the surface of cells, which stimulates the production of other hormones and neurotransmitters. It has also been shown to have antimicrobial properties against bacteria, fungi, and viruses. Adrenalone hydrochloride has a chemical stability that is greater than that of dopamine or adrenaline.</p>

<p>Timapiprant is an amide that acts as a selective inhibitor of the prostanoid receptor CRTH2, which is involved in regulating the inflammatory response. Timapiprant inhibits skin eosinophilia, which is associated with inflammatory skin diseases such as atopic dermatitis and psoriasis. It has been shown to be safe in clinical trials and has a good safety profile. The drug's mechanism of action may be due to its ability to inhibit the production of IL-4 and IL-13 by Th2 cells and its ability to inhibit lung function. Timapiprant has shown efficacy in treating allergic rhinitis, asthma, chronic obstructive pulmonary disease, erythema multiforme, pyoderma gangrenosum, and other types of inflammatory skin diseases.</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>Cyclohexamine hydrochloride is a potent non-selective muscarinic antagonist that has been used as an anesthetic for rodents for the past three decades. It binds to the muscarinic acetylcholine receptors and blocks the effects of acetylcholine, which are involved in regulating heart rate, blood pressure, and other cardiovascular functions. It is also used to treat Alzheimer's disease by blocking acetylcholine from binding to its receptor. Cyclohexamine hydrochloride can cause psychotic symptoms such as hallucinations and delusions when taken in high doses. It may also be toxic to the cerebral cortex when administered at high doses.</p>

<p>Please enquire for more information about [5-(Trifluoromethyl)-1,2-Oxazol-3-Yl]Methanol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Bromoallyl alcohol is a halogenated aromatic hydrocarbon that is an analyte in the chemical analysis of soil. It is also used as a reagent for the debromination of 2-bromopropane and as a dehalogenating agent for the removal of bromine from organic compounds. 2-Bromoallyl alcohol can be distilled at high temperatures, but it will volatilize if heated to 80°C or higher. It has been reported that 2-bromoallyl alcohol was found to be present in all replicates analyzed. The recovery of this compound ranged from 83% to 114%. 2-Bromoallyl alcohol is used as a reagent in organic synthesis, such as in palladium catalyzed couplings with boronic acids and esters. This compound may also be used to synthesize N-(2-hydroxyethyl)hydroxylamines by reacting with sodium hydroxide</p>