Organic Halides

<p>1-[4-(Benzyloxy)phenyl]-2-bromopropan-1-one is an estrogenic compound. It is a reactive substance that can be synthesized by reductive amination of hydroxybenzaldehyde with benzyl bromide. 1-[4-(Benzyloxy)phenyl]-2-bromopropan-1-one has been shown to be metabolized in the liver by cytochrome P450 enzymes to form the corresponding alcohol and carboxylic acid. It binds to estrogen receptors, which may be due to its ability to bind to DNA. The binding of this substance to estrogen receptors may induce transcriptional activation and increase protein synthesis in cells.</p>

Please enquire for more information about N-(2-(3,4-dimethoxyphenyl)ethyl)-2-chloropropanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>CCT 241533 is a Chinese herb that has been shown to have anti-cancer properties. It has been demonstrated to inhibit the growth of HL-60 cells and induce apoptosis in these cells. CCT 241533 also inhibits the proliferation of epidermal growth factor (EGF) and induces cell death in response to radiation. This drug also binds to toll-like receptors, which are proteins on the surface of cells that detect pathogens and initiate an immune response. CCT 241533 has been shown to inhibit polymerase chain reactions by competitive inhibition or by binding to DNA, preventing transcription or replication. CCT 241533 may be useful for the treatment of infectious diseases, such as tuberculosis, because it can bind to bacterial 16S ribosomal RNA and inhibit protein synthesis, leading to cell death by inhibiting the production of proteins vital for cell division.<br>CCT 241533 has been shown in animal studies to be effective against cervical cancer due to its ability to bind</p>

<p>L-Homocysteine thiolactone hydrochloride is a synthetic radiotracer. It has been used as a positron emission tomography (PET) radiopharmaceutical to image brain tumors and other cancers. L-homocysteine thiolactone hydrochloride is synthesized from L-cysteine and aluminium chloride. The yield of this reaction is usually low, but can be increased by addition of sodium hydroxide or tetrabutylammonium bromide. L-homocysteine thiolactone hydrochloride has been shown to be an effective radiotracer for the detection of cancerous tissue in the brain, breast, and prostate.</p>

<p>Please enquire for more information about 3,5-Dichloro-4-hydroxybenzenesulfonyl chloride 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-Chloropropyl)-trimethylammonium chloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Bromo-2-fluoro-1-nitrobenzene is a molecule that has anticancer activity. It inhibits cancer cells, but does not affect normal cells. The mechanism of action of 4-bromo-2-fluoro-1-nitrobenzene is not yet known. However, it may be due to its ability to react with the prenyl group in the cell membrane, which is important for cell growth and division. The human liver metabolizes 4-bromo-2-fluoro-1-nitrobenzene by kinetic and thermodynamic properties. This drug also has pharmacokinetic properties and can be detected in the bloodstream, urine, and feces for up to two weeks after administration. Fatty acid metabolism can cause drug reactions when taken with 4bromo2furo1nitrobenzene. Protein–protein interactions can also lead to side effects when taking this drug, such as enzyme inhibition</p>

3-Fluorophenylpropan-2-amine (3FPPA) is a synthetic, nonselective dopamine and serotonin reuptake inhibitor. 3FPPA has been shown to inhibit the growth of cancer cells in vitro, and enhances the release of growth factors from nerve endings in rat brain slices. 3FPPA can be used as a test compound for investigating the effects of psychostimulants on neural cell division. 3FPPA binds to fatty acids and can be used as a medication to treat obesity or cancer. 3FPPA is not selective for either dopamine or serotonin, but is an analog of both amines.

<p>3,4,5,6-Tetrafluorophthalic acid is a crystalline solid that is used in the synthesis of polycarboxylic acids. It is also an antimicrobial agent that can be used to fight cancer cell lines. 3,4,5,6-Tetrafluorophthalic acid has been shown to inhibit the growth of carcinoma cells and other microorganisms by binding to their DNA and interfering with the production of proteins essential for cell division. 3DCTKP binds to bacterial 16S ribosomal RNA and inhibits protein synthesis. This drug has hydrogen bonding interactions with chlorine atoms and fluorescence properties due to its carbonyl group. The kinetic data for this compound was determined using liquid chromatography method.</p>

1-Butyl-4-methylpyridinium chloride is a pyridine salt that is used for the treatment of osteoporosis. It has been shown to increase the rate of mineralization and reduce the viscosity of beta-amyloid peptide solutions. The biological activity of 1-butyl-4-methylpyridinium chloride has been demonstrated in animal studies, where it was shown to have a significant effect on calcium assays, hydrophilic interaction chromatography, and beta amyloid peptide. This drug also has pharmacokinetic properties that are similar to those of other pyridinium salts. Molecular modeling studies show that 1-butyl-4-methylpyridinium chloride binds well to calcium ions, which may be due to functional groups such as chlorides. This drug also has photocatalytic activity and can be used as a homogeneous catalyst in chromatographic science.

<p>CB1 cannabinoid antagonist, non-CB1/CB2 receptor (GPR55) agonist; anorectic</p>

<p>3-Aminophthalic acid hydrochloride is a diazonium salt that emits light when it reacts with chloride. This compound has been shown to be photophysically active in the presence of human serum, tumor tissue, and micelles. 3-Aminophthalic acid hydrochloride has also been found to be cytotoxic in a number of cancer models. It may also cause death by chemiexcitation of tissues. Furthermore, 3-aminophthalate and acetyl derivatives have shown anticancer activity.</p>

<p>Methyl 4-chlorophenylacetate is an antibacterial agent that belongs to the group of decarboxylated compounds. It has been synthesised and chiral, with a pyruvic acid moiety. Methyl 4-chlorophenylacetate is bactericidal against Pyricularia oryzae and other microorganisms in vitro. It has also been shown to inhibit histamine H1 receptors in rats. The molecular modelling study showed that methyl 4-chlorophenylacetate forms hydrogen bonds with the bacterial cell membrane, which may lead to the formation of pores in the membrane, resulting in cell death.</p>

<p>2,6-Dichloro-1,5-dinitronaphthalene is an organic compound that is used as a reagent for the synthesis of other compounds. It can also be used in research for the synthesis of 2,6-dichloro-1,5-dinitronaphthalene derivatives. The CAS number for this compound is 320600-07-5. This compound is a versatile building block and has many uses as a fine chemical.</p>

Tert-butyl diphenylchlorosilane is a chemical compound that belongs to the group of organosilicon compounds. It is used for the preparation of various organosilicon compounds, such as trifluoroacetic acid, which is used in analytical chemistry. The synthesis of tert-butyl diphenylchlorosilane starts with the reaction between hydrochloric acid and sodium citrate. This yields a phosphate bond and a hydroxyl group. In order to form the desired product, tert-butyl diphenylchlorosilane, this intermediate is reacted with trifluoroacetic acid in an asymmetric synthesis to yield the desired product. The reaction mechanism of this process involves hydrogen chloride as an electrophile attacking the carbonyl carbon atom in trifluoroacetic acid, leading to an elimination reaction. This elimination reaction results in two possible products: tert-butyl acetate or tert-butyl chloros

<p>Heptadecafluoro-N,N-Bis(2-Hydroxyethyl)Octanesulphonamide is a lubricant that is used in the manufacture of polyester films. It is insoluble and has excellent compressive properties. This compound is soluble in both organic solvents and water, and can be applied as a transfer agent or to obviate the need for a separate lubricant. Heptadecafluoro-N,N-Bis(2-Hydroxyethyl)Octanesulphonamide is an inorganic material that does not react with other materials. It also has good deformation resistance and low hardness. The particle size of this compound is between 5 and 10 microns.</p>

Magnesium chloride hexahydrate is a chemical compound with the formula MgCl2·6H2O. It is used as an electrolyte in wastewater treatment and for the production of magnesium metal. The optimum concentration for this chemical is between 0.1-0.3 mol/L, which can be found in nature. Magnesium chloride hexahydrate is also used as a component in dextran sulfate, which is an additive to prevent clumping of particles suspended in water or other liquids. This compound has been shown to affect the activity of enzymes such as xylanase, protease, and amylase. Magnesium chloride hexahydrate has a phase transition temperature of 40 °C and can form coordination geometry structures with copper(II) ions at high temperatures.

<p>Chlorsulfuron is a herbicide that inhibits the enzyme acetolactate synthase. This inhibition prevents plants from synthesizing three essential amino acids, which leads to plant death. Chlorsulfuron has been shown to be highly resistant to photosynthetic activity and transport properties, and it has no effect on soybean extract or chlorsulfuron enzyme activities in vitro. The anhydrous sodium salt of chlorsulfuron is stable in water and other solvents, making it a good choice for analytical methods such as HPLC.</p>

<p>2,4-Dichlorophenoxyacetic acid methyl ester is a herbicide that inhibits the growth of plants by inhibiting photosynthesis. It is an organic compound with a molecular weight of 168.2 g/mol. This product has been shown to biodegrade in soil and water, as well as be non-persistent in the environment. 2,4-Dichlorophenoxyacetic acid methyl ester is also a pesticide that kills plants by blocking the synthesis of chlorophyll and other plant pigments. This product can be used on trees and shrubs for control of broadleaf weeds and grasses.</p>

The drug 4-Amino-5-chloro-2,3-dihydro-N-[1-(3-methoxypropyl)-4-piperidinyl]-7-benzofurancarboxamide (BZP) is a histamine H2 receptor antagonist. It binds to the histamine H2 receptor in the stomach and duodenum, thereby blocking stomach acid production. BZP has been shown to be effective for treating symptoms of constipation or diarrhoea caused by inflammatory bowel disease or abdominal surgery. BZP also reduces the risk of relapse after surgery but does not affect long term efficacy. This drug is not available in the United States and has significant interactions with other drugs and symptoms including constipation, bowel disease, long term efficacy, and analytical method.

Used in the preparation of 5-member heterocycles

<p>2-Chloro-5-methyl-1,3-benzoxazole (CMB) is a regioselective synthetic intermediate that can be used to synthesize other compounds. It is produced by the reaction of chloromethyl methyl ether with anhydrous magnesium chloride in the presence of a solvent such as THF or diethyl ether. CMB can also be prepared by the reaction of 2,4,6-trichlorobenzoyl chloride with magnesium metal and a solvent such as THF or diethyl ether. This intermediate can be used in cross-coupling reactions with Grignard reagents to produce different compounds.</p>

<p>3-Cyano-5-bromopyridine is an enantiopure organic compound that belongs to the group of halides. It is a functional group that is a reagent in organic synthesis, and it can be used as a precursor to dyestuffs. 3-Cyano-5-bromopyridine has been shown to have antimicrobial activity against bacteria and fungi. It also has a metabotropic glutamate receptor subtype selective affinity, which may be due to its ability to bind with glutamate in complex molecules.</p>

<p>3-Chloropropionic acid is a non-toxic organic compound that exhibits significant cytotoxicity against many bacterial strains. It is a white solid, which is soluble in water and has no odor. 3-Chloropropionic acid can be synthesized by the reaction of malonic acid with ethylene diamine or by the reaction of bromoacetic acid with sodium salts. The optimum pH for this reaction is 6.5 to 7.5 and the optimum temperature is 25°C to 30°C. This compound has been shown to inhibit the synthesis of fatty acids in bacteria, which may be due to its hydroxyl group. 3-Chloropropionic acid reacts with trifluoroacetic acid, giving an ester product, which can then be hydrolyzed back to 3-chloropropionic acid. This chemical also has a physiological function as an intermediate in the synthesis of other chemicals such as biotin and pantothen</p>

<p>Please enquire for more information about 2-Chloro-N-(3-chloro-4-methylphenyl)propanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>20-Fluoromibolerone is a fluorinated analogue of the natural hormone mibolerone. It has been shown to have affinity for prostate tissue and to be selective for cancer cells in vivo, when injected into rats. The uptake of 20-fluoromibolerone into tissues is very high, with preferential accumulation in the liver, kidney and prostate. This drug is metabolized by sulfation and excreted in the urine as sulfate and positron. 20-Fluoromibolerone also has been shown to have a strong affinity for bone, which may be due to its ability to accumulate in bone tissue.</p>

<p>2,5-Dichloro-4-ethoxybenzenesulfonyl chloride is a chlorosulfonyl reagent that is used in the synthesis of organic compounds. It can be used as a building block, a research chemical, or an intermediate compound. This material has been shown to be useful in the synthesis of many different types of compounds and it provides a versatile scaffold for chemical reactions. The reaction component has shown high quality and was obtained from a reliable source.</p>

<p>4-Fluoro-2-(trifluoromethyl)phenol is a reactive compound that can be used for the synthesis of a variety of functionalized molecules. It is prepared by a cross-coupling reaction with an organometallic reagent and a chloride such as methylene chloride or chloroform. The 4-fluoro group on the phenol provides the desired electrophilic character to react with electron rich nucleophiles, such as an allylbenzene or styrene. The product of this reaction is an alkylating agent that has been shown to have signalling properties, operational capabilities, and fabricating benefits.</p>

<p>6-Chloroisatin is a potent inhibitor of bacterial growth that binds to the 50S ribosomal subunit. It has been shown to have strong inhibitory activity against tuberculosis and sulphamethoxazole-resistant strains of Mycobacterium tuberculosis. 6-Chloroisatin inhibits bacterial growth by binding to the 50S ribosomal subunit, thereby preventing protein synthesis and cell division. The electron deficient form of 6-chloroisatin reacts with the electron rich sulphamethoxazole by displacement of chloride ion from the sulphonamide ring, forming a regiospecific product that inhibits bacterial respiration. This reaction system is inhibited by activated carbon, which may be a potential therapeutic strategy for patients with drug resistant tuberculosis.</p>

<p>2-Chloro-3-nitrobenzonitrile is a high quality, reagent, and complex compound that is useful as an intermediate for the synthesis of fine chemicals. It has CAS No. 34662-24-3 and can be obtained from chemical suppliers worldwide. The compound is also useful as a building block for the synthesis of pharmaceuticals and other speciality chemicals. 2-Chloro-3-nitrobenzonitrile is a versatile building block that can be used in organic reactions to produce research chemicals such as derivatives of indole or phenol compounds.</p>

<p>Chlorfluazuron is a pesticide that inhibits the activity of an enzyme, amino transferase, which is involved in nitrogen metabolism. Chlorfluazuron has been shown to be effective against a wide range of insects and weeds. It is used for the control of pests on crops such as cotton, soybean, corn, sorghum, wheat, rice and vegetables. Chlorfluazuron also has a synergistic effect with other pesticides such as carbaryl and pyrethroid.</p>

<p>2-(Bromomethyl)-1-methylpyrrolidine HBr is a high quality, reagent grade compound that belongs to the category of complex compounds. It is an intermediate for the production of fine chemicals and speciality chemicals. 2-(Bromomethyl)-1-methylpyrrolidine HBr has been found to be a useful scaffold for the synthesis of various bioactive molecules, including pharmaceuticals, natural products and agrochemicals. This compound is also a versatile building block that can be used in reactions in order to produce high quality compounds.</p>

3-Chloro-4-fluorobenzoic acid is a prodrug that is converted to fluvoxamine maleate, its active form, by esterases. It is an inhibitor of the enzyme nitric oxide synthase and is used in the treatment of cancer. 3-Chloro-4-fluorobenzoic acid has been shown to inhibit cellular growth and proliferation in cancer cells. The molecular modeling study showed that 3-chloro-4-fluorobenzoic acid binds to the kinesin motor domain in a manner similar to fluvoxamine maleate but has a lower inhibitory potency than fluvoxamine maleate. Nonetheless, it was found that 3-chloro-4-fluorobenzoic acid could be used as a prodrug for fluvoxamine maleate.

<p>4-Chlorocinnamic acid is a malonic acid derivative and one of the cinnamic acid derivatives that has been shown to inhibit many chemical reactions. It inhibits the production of tyrosinase, which is an enzyme that catalyzes the conversion of tyrosinase to 4-hydroxycinnamic acid. 4-Chlorocinnamic acid also inhibits the growth of Candida glabrata in vitro. The effect on candida is due to its ability to inhibit the production of hydroxyl group and aromatic hydrocarbon, both of which are required for candida's survival. 4-Chlorocinnamic acid binds with aryl halide and neutral ph, preventing it from reacting with other substances.</p>

3-Bromo lidocaine is a useful building block for the synthesis of complex compounds. It is a chemical intermediate that is used in the manufacture of pharmaceuticals and other organic chemicals. 3-Bromo lidocaine has a CAS number of 1044658-01-6, which identifies it as a reagent that can be used in organic synthesis. It is an important reaction component with high quality and versatility, making it an excellent choice for research chemical or speciality chemical purposes.

<p>3-Bromo-4-methoxyphenylacetic acid is a benzyl ester of hydroxybenzoic acid. It is used as a synthetic precursor for the synthesis of curare and related compounds. 3-Bromo-4-methoxyphenylacetic acid was first synthesized in 1869 by German chemist Wilhelm Koenigs and has been widely used as a synthetic intermediate in organic chemistry. This compound can be prepared from bromobenzene, methoxybenzene, and acetic acid in the presence of dimethyl ether or nitrite. 3-Bromo-4-methoxyphenylacetic acid is also used to produce nitromethane, an alkylating agent that reacts with amines, alcohols, thiols, and sulfides to form N-substituted nitro compounds.</p>

<p>3-Fluorocinnamic acid is an organic compound that belongs to the class of amides. It reacts with metal ions such as copper, silver, or gold. 3-Fluorocinnamic acid has a constant boiling point and can be used in the preparation of cinnamic acid derivatives. 3-Fluorocinnamic acid also has redox potential and is used as a substrate in enzyme preparations. 3-Fluorocinnamic acid can be synthesized by hydrolysis of malonic acid and metal salts with hydrochloric acid, which then reacts with triticum aestivum. The product is purified by recrystallization from water. This compound inhibits the reaction that converts lactose into glucose and galactose, leading to the production of lactic acid from milk.</p>

<p>2-bromo-5-iodoanisole (BIA) is an aryl halide that undergoes electrophilic substitution reactions. It has been used as a chlorinating agent to produce monochlorobenzene, dichlorobenzene, and trichlorobenzene. 2-bromo-5-iodoanisole can also be used to synthesize butyllithiums and mesylates. These compounds are bifunctional, meaning they can act as both an electrophile and a nucleophile in substitution reactions. When 2-bromo-5-iodoanisole reacts with methoxy groups, it forms the highly reactive fluorine compound which then activates the aromatic heterocycles.<br>2-bromo-5-iodoanisole is labile, meaning that it easily undergoes hydrolysis or other chemical reactions. This reactivity makes 2BIA useful for organic synthesis because it can</p>

<p>4-Methoxyphenylmagnesium bromide - 0.5M solution in THF is a cytotoxic agent that binds to the estrogen receptor, which is involved in breast cancer cell proliferation and differentiation. It is an azide that has been shown to react with hydrochloric acid to form an amide. This reaction may be stereoselective and involve dehydration of the amine group. The mechanism of this reaction involves the formation of a trifluoroacetic acid derivative, which undergoes unsaturated alkyl halogenation followed by chloride ion attack on the double bond. 4-Methoxyphenylmagnesium bromide - 0.5M solution in THF has been shown to inhibit the proliferation of human MCF-7 breast cancer cells, as well as other estrogen receptor modulators such as amines and trifluoroacetic acid.</p>

<p>Apelin-17 trifluoroacetate is a reaction component, reagent and useful scaffold for the synthesis of complex compounds. It is a high quality, research chemical that is used in the synthesis of fine chemicals. Apelin-17 trifluoroacetate has versatile building block and can be used as a useful intermediate or as a speciality chemical. It also has high reactivity and is soluble in organic solvents.</p>

<p>Tetraethyl difluoromethylenebisphosphonate (Tefd) reacts with nucleophiles, such as alcohols and amines, to form tetraethyl pyrophosphate (TEPP), which is a powerful phosphorylating agent. TEPP has been used for the efficient synthesis of esters and amides from alcohols and amines, respectively. Tefd is also used in the synthesis of pyrophosphates from carboxylic acids.</p>

<p>O-Fluorobenzyl alcohol is a compound with the chemical formula of C6H5FO. It is a colorless liquid with a sweet odor and tastes like ether. This compound is soluble in water, ethanol, and acetone. O-Fluorobenzyl alcohol has been used as an analytical reagent for the determination of protonated molecules such as phenols or carbohydrates. It also has cytotoxic properties, which have been shown to be effective against cancer cells. O-Fluorobenzyl alcohol acts as a γ-secretase inhibitor by binding to the catalytic site of the enzyme, preventing proteolytic cleavage of amyloid precursor protein (APP) and subsequent production of amyloid β peptide (Aβ).</p>

<p>3-Fluoro-4-hydroxyphenylpropanenitrile is a reagent and building block for chemical synthesis, with potential applications in the manufacture of pharmaceuticals, agrochemicals, and fine chemicals. 3-Fluoro-4-hydroxyphenylpropanenitrile is an important intermediate or building block in organic synthesis due to its versatility and variety of reactions. In particular, it can be used as a starting material for the synthesis of new compounds or as a building block in complex syntheses. 3-Fluoro-4-hydroxyphenylpropanenitrile has been reported to be useful in the preparation of many complex molecules including fluoroquinolones, nitrile oxides, and azole antifungals.</p>

Please enquire for more information about N-1,3-Benzodioxol-5-yl-2-chloroacetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

1-Bromo-3,4,5-trimethoxybenzene is a brominated molecule that is used in the synthesis of other organic compounds. It inhibits protein synthesis by inhibiting the production of ribosomes and is toxic to cancer cells. It has been shown to have inhibitory properties against the growth of k562 cells, which are leukemia cells. The mechanism by which 1-bromo-3,4,5-trimethoxybenzene inhibits protein synthesis is not fully understood. However, it has been found that this compound inhibits DNA polymerase activity and prevents RNA polymerase from transcribing genetic information from DNA to mRNA. This may be due to its ability to act as a diazonium salt or an n-dimethyl formamide substrate. In addition, 1-bromo-3,4,5-trimethoxybenzene can be hydrolyzed into trimethoxybenzene and b

<p>8-Chloro-5,10-dihydro-11H-dibenzo[b,e][1,4]-diazepin-11-one is a polycyclic multicyclic compound that has stable properties. It is an atypical antipsychotic and antidepressant with high stability. This drug can be prepared by the process of optimization of reaction time and is an orthogonal molecule to typical antipsychotics. 8CBDD can be used in the preparation of atypical antipsychotics and antidepressants.</p>

<p>7-Amino-5-chloro-2(3H)-benzoxazolone is a high quality, versatile building block that has been used in the synthesis of many complex compounds. It has been used as an intermediate for the synthesis of reagents and fine chemicals. 7-Amino-5-chloro-2(3H)-benzoxazolone can be used as a speciality chemical and research chemical. CAS No. 889884-60-0.</p>

<p>Please enquire for more information about 5-Amino-4-oxopentanoic acid benzyl ester hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1,1,2,2,3,3,4,4-Octafluoro-1,4-Bis[(1,1,1,2,3,3-Heptafluoro-2-propanyl)oxy]butane is a signal that has been used for demographic and population modelling. Gravity modelling is one of the techniques that has been used to analyse this signal. Regression techniques have also been used to analyse this data set. This signal has shown disparities between different parameters in test results.</p>

<p>2-(2,5-Dichlorophenyl)ethanol (2,5-DCPE) is an organic chemical that is used as a building block for the synthesis of fine chemicals and pharmaceuticals. 2,5-DCPE can be used as a reactant in synthesizing more complex compounds. It reacts with many different functional groups to form covalent bonds. The compound has been shown to have high quality and has been characterized by nuclear magnetic resonance spectroscopy and mass spectroscopy.</p>

<p>Tetrafluoro-2-(tetrafluoro-2-iodoethoxy)ethanesulfonyl fluoride (TFEI) is a fluorinated solvent that has been used in the manufacture of organic thin films. TFEI is a colorless liquid with a strong, unpleasant odor. It is soluble in water and has a boiling point of about 140°C. TFEI possesses good thermal stability and can be used as an etchant for silicon or glass surfaces. TFEI is also capable of dissolving polymers such as polyimide, polyamide, polyethylene terephthalate, and polystyrene.<br>TFEI has been shown to be highly toxic to bacteria and fungi and can be used as an antimicrobial agent in household cleaners, paints, adhesives, varnishes, plastics, textiles, and other industrial products.</p>

2-Bromo-3'-bromoacetophenone is a chemical compound that can be used as an oxidant in organic synthesis. It is a brominated phenol derivative, which undergoes bond cleavage to produce benzoylbenzene and acetone. The reaction is mediated by potassium permanganate in the presence of oxygen. X-ray crystallography and crystallography have been used to identify the molecular structure of 2-bromo-3'-bromoacetophenone. The yield for this reaction is high and can be increased by using solvents such as ethanol or tetrahydrofuran and a reaction time of 1 hour at 100°C.

<p>N,N'-4,4'-Bis(benzyl-2-boronic acid)-bipyridinium dibromide is a high quality reagent that can be used as an intermediate for the synthesis of complex organic compounds. It is a complex compound that contains boronic acid and bipyridinium moieties. N,N'-4,4'-Bis(benzyl-2-boronic acid)-bipyridinium dibromide is useful in the synthesis of fine chemicals and speciality chemicals. It has versatile building block properties and can be used as a reaction component in many chemical reactions.</p>

<p>3-Chloro-4-hydroxycinnamic acid is a coelicolor biosynthetic precursor that is synthesized from 4-hydroxycinnamic acid and chlorinated. It can be used for the synthesis of aminocoumarin moieties and other prenylated molecules. 3-Chloro-4-hydroxycinnamic acid has been shown to be an effective inhibitor of streptomyces coelicolor, which is a type of bacterium that produces antibiotics. The gene responsible for the biosynthesis of 3-chloro-4-hydroxycinnamic acid has also been identified in streptomyces clorobiocin, which is another type of bacterium that produces antibiotics.</p>

4-Amino-2-chlorophenol is an aminophenol that is used in the production of acetate, which is used in the manufacture of acetic acid. It is also used as a building block for organic synthesis. 4-Amino-2-chlorophenol reacts with acetyl chloride to form chloracetyl chloride, which can then be reacted with piperonyl butoxide to form 2-(4'-aminophenyl)-4,6-dichloropyridine. This reaction is catalyzed by hydrogen chloride and hydrogen bond formation with urea nitrogen. 4-Amino-2-chlorophenol has been shown to have long-term toxicity in animal studies and may be toxic when inhaled or ingested.

<p>3-Trifluoromethylbutyric acid is a synthetic compound that has been studied as a potential drug for the treatment of dyslipidemia. 3-Trifluoromethylbutyric acid binds to the enzyme phosphatase, which is a key regulator of lipid metabolism and controls the production of lipids in cells. This binding prevents the phosphatase from breaking down phosphoinositides, leading to an increase in the levels of phosphoinositides. The resulting increase in the levels of these molecules causes an increase in the number of insulin receptors on cell surfaces and leads to an improvement in insulin sensitivity. 3-Trifluoromethylbutyric acid also has binding sites on human cells that are specific for subtype 7, which is associated with lower risk for cardiovascular disease, obesity, and diabetes.</p>

Please enquire for more information about N-(1,4-Benzodioxan-2-carbonyl)-piperazine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-[4-[(1Z)-4-Chloro-1,2-diphenyl-1-buten-1-yl]phenoxy]ethanol is a selective estrogen receptor modulator that has been shown to inhibit the growth of breast cancer cells in mice. It binds to the estrogen receptor (ER) and inhibits its transcriptional activity by competing with estradiol for binding. 2-[4-[(1Z)-4-Chloro-1,2-diphenyl-1-buten-1-yl]phenoxy]ethanol can be used as a postmenopausal hormonal therapy in women who are at an increased risk for breast cancer. This drug has been shown to have genotoxic activity and may cause dyspareunia and carcinogenic potential.

<p>Methyl (1R,2S,3S,5S)-3-(4-fluorophenyl)-8-[(E)-3-iodoprop-2-enyl]-8-azabicyclo[3.2.1]octane-2-carboxylate is an imaging agent that is used to diagnose and treat bowel diseases. It has pharmacokinetic properties that allow for a more accurate diagnosis of eye disorders and bowel disease. Methyl (1R,2S,3S,5S)-3-(4-fluorophenyl)-8-[(E)-3-iodoprop-2-enyl]-8-azabicyclo[3.2.1]octane-2-carboxylate is a DPPIV inhibitor that modulates the dopamine transporter in the brain by binding to its extracellular site of action on dopamine transporter proteins and blocking the reuptake of dopamine into the pres</p>

<p>S-(trifluoromethyl)-L-homocysteine is a chemical compound that belongs to the group of antimicrobial agents. It is an inhibitor of bacterial growth and can be used to treat infectious diseases caused by bacteria. S-(Trifluoromethyl)-L-homocysteine inhibits the synthesis of methionine by binding to corynebacterium glutamicum and preventing the formation of methionine from homocysteine. This compound has shown structural analysis in wild-type strains and synthetase mutations, which have revealed its hydrogen bonding interactions with trifluoroacetic acid and ph optimum. Chemical stability has also been demonstrated for this compound in the presence of various acids, bases, alcohols, and oxidizing agents.</p>

<p>IR-775 chloride is a fluorescent agent that can be used for both diagnostic and therapeutic purposes. It is used in the detection of cells, proteins, and nucleic acids. IR-775 chloride has a hydrophobic nature, which allows it to bind to molecules that are hydrophobic themselves. It can also be used as a ligand for the attachment of other molecules with complementary properties, such as β-cyclodextrin, which is an example of a heterobifunctional molecule. This property gives IR-775 chloride an advantage over other fluorescent agents due to its ability to transport molecules through cell membranes. The diameter of IR-775 chloride is approximately 10 nm, making it useful in microscopy techniques such as fluorescence microscopy and confocal microscopy.</p>

<p>Creatine zinc chloride is a basic protein that is metabolized to creatinine and guanidinoacetate. Creatine zinc chloride has been shown to inhibit the mitochondrial membrane potential, leading to the inhibition of cardiac muscle contraction and myocardial infarct size. Creatine zinc chloride also has physiological functions in energy metabolism, cytosolic calcium regulation, and glomerular filtration rate. Creatine zinc chloride may be used for the treatment of metabolic disorders, such as obesity and diabetes mellitus type II.</p>

<p>2-Bromobenzoyl chloride (2BB) is an aromatic hydrocarbon that can be used to synthesize a variety of organic compounds. 2BB has been shown to have cytotoxic activity in vitro, but it is not yet known what the mechanism of action is. In addition, 2BB binds to DNA and RNA, and it has been used as a reagent for the synthesis of phenyl groups. The compound also reacts with copper or carbonate ions to form bromocarbenes or chlorocarbenes respectively. 2BB is also used for the Friedel-Crafts reaction, Suzuki coupling reaction, and acylation reactions.</p>

Perfluoro-2,5-dimethyl-3,6-dioxanonanoic acid (PFDA) is an activated perfluoroalkyl substance that has been shown to be toxic in animal studies. PFDA is a fluorinated organic compound that does not contain chlorine. It belongs to the group of polyfluoroalkyl substances and is used as a solvent in the manufacture of semiconductors and other electronic devices. PFDA can enter the environment through wastewater treatment plants or by atmospheric deposition. PFDA is found in drinking water, food, and human blood samples at low levels. PFDA has been shown to have health effects on laboratory animals and humans such as changes in thyroid hormone levels, decreased fertility rates, increased cholesterol levels, liver damage, and developmental toxicity.

<p>1,1,1-Trifluoro-2-propanol (TFHP) is a molecule that contains three hydrogen atoms and two fluorine atoms. It has a frequency shift of 0.00116 cm−1 in the infrared spectrum due to the conformational properties of its hydroxyl group, which causes the OH stretching vibration to be shifted. TFHP is a weak acid that reacts with sodium trifluoroacetate to form trifluoroacetic acid and hydroxyl ions. TFHP has been shown to have biological properties in bacteria, such as inhibiting bacterial growth and suppressing protein synthesis. The molecular structure of TFHP is made up of a hydrogen atom on each nitrogen atom, which is then bonded to an intramolecular hydrogen bond and an intermolecular hydrogen bond with other TFHP molecules. The deuterium isotope can also be found in this compound, which will cause a shift in IR frequency from 0.00116 cm</p>

<p>7-Bromo-9H-fluoren-2-amine is a constant analog of the naturally occurring hormone progesterone. It is used in biological studies as a fluorescence probe for the study of progesterone receptor. 7-Bromo-9H-fluoren-2-amine has been shown to have efficient absorption and emission spectra, as well as photophysical properties. This compound has been shown to enhance the fluorescence of other molecules, such as amines, which may be due to its ability to act as an energy transfer agent. This chemical has also been shown to be pharmacokinetically active and increase the fluorescence emissions from cells in culture.</p>

4'-Chloro-4-methoxychalcone is a dihedral molecule that has been studied by laser spectroscopy. The wavelength and efficiency of the laser have been shown to be dependent on the chalcone's dipole moment. Chalcones are also used in the synthesis of other compounds, such as benzene, which is an aromatic hydrocarbon. Chalcones are used as optical brighteners in detergents and soaps and can also be used to induce evaporation of organic solvents. 4'-Chloro-4-methoxychalcone is used as an intermediate in crystal x-ray diffraction studies.

<p>4-Chlorophenylhydrazine hydrochloride is a chemical compound that contains a pyrazole ring, chlorine and anhydrous sodium. This substance is used as a reactant in the production of diazonium salts. 4-Chlorophenylhydrazine hydrochloride also inhibits the reaction of benzodiazepines with their binding site on the GABA receptor, which prevents the formation of reactive intermediates. It has been shown to have an inhibitory effect on wastewater treatment and can be used for the treatment of acidic water. 4-Chlorophenylhydrazine hydrochloride reacts with fluorescence probes to form intermolecular hydrogen bonds and hydrogen bonds that are used for determining pH values in solution.</p>

<p>Please enquire for more information about 2-(3-Fluorophenyl)thiazole-4-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Fluorescent Brightener 191 is a monomer that can be used in the textile industry to increase brightness and fluorescence of textiles. It is water soluble, non-toxic, and stable. The impurities of this product are monitored by testing for chloride ion content. Fluorescent Brightener 191 is also used for effervescent and osmosis control in water treatment plants, as well as clarification of wastewater effluent. Its fluorescence properties make it an ideal choice for monitoring the presence of substances, such as chloride ions, in solution by measuring the intensity of light emitted from a sample. Fluorescent Brightener 191 is also known to have a high solubility in organic solvents such as chloroform or acetone, which makes it suitable for labeling purposes.</p>

3-Hydroxy-4-methoxybenzylamine hydrochloride is a vanilloid receptor 1 (VR1) antagonist. It has been shown to inhibit the growth of prostate cancer cells in cell-based assays and to have potential as a therapeutic for prostate cancer patients with high triglycerides. 3-Hydroxy-4-methoxybenzylamine hydrochloride is also an inhibitor of guanosine, which is involved in the production of energy. It has been shown to enhance the antitumor effects of cetuximab, an antibody that targets the epidermal growth factor receptor (EGFR). 3-Hydroxy-4-methoxybenzylamine hydrochloride is soluble in water and can be used as a solvent for other compounds. 3-Hydroxy-4-methoxybenzylamine hydrochloride is also known by its chemical name, N-(3,4 dimethylphenyl)-

<p>5-Chloro-2-methoxy-4-methylnitrobenzene is a high quality chemical that can be used as a research chemical, reagent, or a useful scaffold. It is also an intermediate in the synthesis of organic compounds. 5-Chloro-2-methoxy-4-methylnitrobenzene is a versatile building block for the synthesis of other chemicals and has many uses in the pharmaceutical industry. The CAS number for this chemical is 101080-03-9.</p>

Please enquire for more information about Ethyl 5-chloropyrazolo[1,5-a]pyrimidine-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>3-Chloro-N-methyl-5-(trifluoromethyl)-2-pyridinamine is a fine chemical that is used as a versatile building block for the synthesis of other chemical compounds. 3-Chloro-N-methyl-5-(trifluoromethyl)-2-pyridinamine is also useful as an intermediate in research and development, and can be used to produce speciality chemicals. This compound has shown to be a useful reagent and is of high quality.</p>

3-[4-(trifluoromethoxy)phenyl]propanoic acid (TFPA) is a versatile building block that can be used as a reagent and research chemical. TFPA has the potential to be used as a useful intermediate in the synthesis of complex compounds and useful scaffolds. It also has been shown to have high quality, which makes it an excellent choice for use in reactions. This compound is also useful for creating speciality chemicals.

<p>5,6-Dichloroindole is a chemical compound that contains a functional group with acidic properties. The compound has been shown to inhibit the activity of bafilomycin A1, which is an inhibitor of vacuolar ATPase. This inhibition leads to an increase in intracellular phosphate levels and an accumulation of lysosomal membrane proteins. 5,6-Dichloroindole has also been found to inhibit bone resorption in gramine-fed rats. It also has anti-inflammatory effects and inhibits the growth of zoobotryon pinnatum cells and algal cells. 5,6-Dichloroindole can be used as a molecular descriptor for predicting the presence or absence of bryozoan species in a sample.</p>

<p>Hydrochlorothiazide is a thiazide-sensitive NaCl cotransporter inhibitor. Due to its diuretic properties, hydrochlorothiazide can inhibit the transport of sodium chloride in the distal tubule in the nephron and, as a consequence, the concentration of Na is decreased. In combination with other substances, such as captopril, hydrochlorothiazide acts an antihypertensive to reduce high blood pressure.</p>

2-Chloro-5-nitroacetophenone is a synthetic chemical that is used in the synthesis of vismodegib. It has been shown to have pharmacokinetic properties, such as a low clearance and high volume of distribution. A number of impurities are found in this chemical, including halide ions, amines, and benzofuran derivatives. 2-Chloro-5-nitroacetophenone is genotoxic and can cause cancer. This chemical should not be exposed to radiation or chlorine gas.

Racemic trans-N-desmethyl sertraline hydrochloride, also known as desmethylsertraline or N-desmethylsertraline, is a member of the selective serotonin reuptake inhibitor (SSRI) class of antidepressants. It has been found to have nootropic effects in animal studies and to attenuate some of the behavioural effects of amphetamine in rats. Racemic trans-N-desmethyl sertraline hydrochloride is a chiral compound with two enantiomers, ("R")-(+)-trans-N-desmethyl sertraline and ("S")-(−)-trans-N-desmethyl sertraline, which are mirror images of each other. The drug is marketed as a racemate; however, only the "R" enantiomer is active. Racemic trans-N-desmethyl sertraline hydrochloride has not been shown to produce any clinically significant drug interactions.

<p>2,2,2-Trifluoro-n-phenylacetamide is a functionalized trifluoroacetic acid. It is inactive and can be used for diagnostic purposes. 2,2,2-Trifluoro-n-phenylacetamide reacts with amines to form the corresponding deuterium isotope labeled amine. The heterocyclic amines that are formed react with diazonium salt to produce an enolate anion that reacts with chloride to form the corresponding carboxylic acid derivative. The proton of the carboxylic acid leaves as a protonated ammonium ion, which is stable in alkaline solutions. Amides have a negative charge on the nitrogen atom due to its electron withdrawing properties.</p>

Potassium 4-fluorophenyl glycinate is a compound that has the potential for use as a building block in organic synthesis. It can be used as an intermediate in the synthesis of various other compounds, and is also useful as a reagent in organic reactions. Potassium 4-fluorophenyl glycinate is also used in research to develop new therapeutic agents. This compound has a number of applications, including being used as a building block for pharmaceuticals, agrochemicals, and specialty chemicals.

2-[[1-Methyl-2-[3-(Trifluoromethyl)Phenyl]Ethyl]Amino]Ethyl (2ME2EAE) is a natriuretic drug that is used to treat congestive heart failure. It has been shown to reduce the production of brain natriuretic peptide (BNP) by the kidneys and to increase blood flow in the lungs. 2ME2EAE has also been shown to have positive effects on blood pressure, glycerides, and fatty acid levels in animals with congestive heart failure. 2ME2EAE can be taken orally or injected into the pleural cavity. It should not be given intravenously as it may cause kidney damage.

<p>2-Chloro-1,3-difluoropropane (DFC) is a fluorocarbon that is used as an adsorbent for the removal of chlorocarbons. It has a linear structure and is often used in chromatographic analysis. DFC is insoluble in water, but soluble in more polar solvents such as acetone and ether. It also has excellent retention properties for chlorocarbons, which allows it to be used for the separation of halocarbons from fluids.</p>

<p>Amyloid beta peptide (Aβ) is a neurotrophic factor that is involved in the pathogenic mechanism of Alzheimer's disease. This drug inhibits the production of Aβ by binding to the enzyme, secretase. It has been shown that Aβ binds to a transporter protein and is transported into cells, where it accumulates in the cytoplasm. The physiological levels of Aβ are regulated by proteins called "gene chaperones" which prevent Aβ from aggregating into plaques. Dextran sulfate inhibits this process by binding to amyloid and preventing it from accumulating in the cytoplasm. Amyloid beta peptide trifluoroxalate (ATFX) has been shown to inhibit the production of Aβ with structural analysis, inhibition of cellular uptake and secretion, and inhibition of fibrillization. ATFX also has potential as a biomarker for Alzheimer's disease because it can be detected at low concentrations in urine or serum</p>

Etoricoxib is a cyclooxygenase-2 (COX-2) inhibitor, which is a type of nonsteroidal anti-inflammatory drug (NSAID). It works by blocking the enzyme COX-2 that is involved in the production of certain hormones called prostaglandins. These hormones are involved in the inflammation (swelling and heat) associated with conditions such as arthritis. By blocking the action of the COX-2 enzyme, etoricoxib reduces the production of prostaglandins and thus, reduces the inflammation and pain. It has been observed that Etoricoxib shows a higher selectivity for COX-2 over COX-1 in diverse studies, with a COX-1/COX-2 IC50 ratio of 344 for in vitro assays, and it is involved in the modulation of NF-ΚB/COX-2/PGE2 signaling.