Ciano-, nitrilo-

<p>Applications 4-cyano-N,N-dimethylbenzamide (cas# 24167-50-8) is a useful research chemical.<br></p>

<p>Stability Moisture Sensitive<br>Applications 2-phenyl-2-[(trimethylsilyl)oxy]acetonitrile (cas# 25438-37-3) is a useful research chemical.<br></p>

<p>Applications 1,4-Dicyanobenzene is used in the preparation of aryl nitriles.<br>References Lee, H.G., et. al.: J. Am. Chem. Soc., 137, 648 (2015)<br></p>

<p>Applications Phenoxyacetonitrile is a building block that has been used as a reactant for the preparation of [[(oxo)pyridazinyl]phenoxy]acetonitrile derivatives to be used as vasodilators.<br>References Bansal, R., et. al.: Drug Dev. Ind. Pharm., 74, 296 (2013)<br></p>

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<p>Ethyl (Ethoxymethylene) cyanoacetate is a chemical compound that belongs to the family of aldehyde compounds. It is a colorless liquid at room temperature, with an odor similar to that of acetic acid. The compound has been used in the synthesis of epidermal growth factor and diazonium salts. It has also been used in the production of anti-cancer drugs such as malonic acid, which inhibits tumor growth by inhibiting protein synthesis. Ethyl (Ethoxymethylene) cyanoacetate reacts with quinoline derivatives to form carbon disulphide, which can be used as an antimicrobial agent and insecticide.</p>

<p>4-Fluoro-3-nitrophenylacetonitrile is a monomer that can be synthesised from the reaction of carbamic acid and diphenyl ether. It is chiral, stereoselective and nucleophilic. 4-Fluoro-3-nitrophenylacetonitrile can also be synthesised by reacting fluoroacetamide with sodium cyanide in water, forming the corresponding amide, which reacts with acetonitrile to form the nitro compound. The anti-cancer properties of 4-fluoro-3 nitrophenylacetonitrile have been studied in vitro and in vivo. This substance has been shown to inhibit growth of cancer cells and induce apoptosis. In addition, this substance has been used as a synthetic strategy for dihydroisoquinolines, which are important for their anti-cancer properties.</p>

<p>2,5-Difluoro-7,7,8,8-tetracyanoquinodimethane is a donor molecule that has an acceptor property. It can be used in the fabrication of organic light emitting devices. 2,5-Difluoro-7,7,8,8-tetracyanoquinodimethane is a molecule with a molecular structure that consists of two benzene rings and two quinonediimide groups. The molecule has a fluorine atom at position 5 and another fluorine atom at position 8. This molecule has been shown to have good transport properties and to emit light when irradiated with UV radiation.</p>

<p>Cyanomethylenetributylphosphorane (CMTP) is an agent used for the diagnosis of body formation. It is a chemical compound that can be used to produce images of tissue and organs by detecting apoptosis, or programmed cell death. CMTP binds to the glucose-dependent insulinotropic polypeptide receptor (GIPR), stimulating the release of insulin in the pancreas. CMTP also has therapeutic potential for metabolic disorders, as it has been shown to reduce triglycerides and increase HDL cholesterol levels in human serum. CMTP is synthesized from trifluoroacetic acid, which is then reacted with a cyclic peptide containing an amino acid derivative and 1-methyl-2-pyrrolidinone. This reaction produces a molecule with one free amino group at one end and two free carboxylic acid groups at the other end. The molecule can be reacted with epidermal growth factor (EGF) or insulin to</p>

<p>a-Acetylphenylacetonitrile is a bifunctional molecule that can be used in the synthesis of new compounds, such as pharmaceuticals, dyes, and perfumes. It is an analytical technique for measuring the concentrations of cyanides in wastewater. The fluorescence properties of this compound are helpful in detecting the presence of phenylacetone by using a kinetic assay. This compound can also be used to synthesize other organic compounds with high enantiopurity.</p>

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<p>Thiophene-3-acetonitrile is a reactive intermediate that is used in the synthesis of active enzymes. It has been shown to be an efficient method for the synthesis of antitubercular agents, such as rifamycins and other drugs. Thiophene-3-acetonitrile is an electron acceptor and can be used to generate active enzymes, such as those involved in DNA replication and transcription. This compound also has a variety of functional groups, which can be used for a number of techniques, including coordination geometry studies.</p>

<p>Please enquire for more information about (5R)-6-Cyano-5-hydroxy-3-oxo-hexanoic acid tert-butyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-(Dicyanomethylene)-2-tert-butyl-6-(1,1,7,7-tetramethyljulolidinium) (DCJTB) is a red fluorescent dye that emits light when activated by heat. DCJTB is cationic and can be polymerized thermally or chemically. The molecule has been shown to be activated by the addition of an electron donor such as a metal chelate. This reaction takes place in the solution phase. DCJTB has been used for the diagnosis of nonpolar solvents such as gasoline and oil leaks in machine parts. DCJTB has also been used to detect groundwater contamination with trichloroethylene (TCE).</p>

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

<p>Methoxyacetonitrile is a chemical that is used in the manufacture of acrylate polymers. Acrylate polymers are used in animal health, such as plastics for veterinary use and as a coating on animal feed. Methoxyacetonitrile can be used to create a cationic polymerization reaction with an organic solution. The resulting polymer film has been shown to have good chemical stability. Productivity depends on the temperature and size of the particles, which can be controlled with an electric field or by changing the concentration of reactants. Methoxyacetonitrile may also be used as a dietary supplement because it has been shown to provide relief from chronic coughs.</p>

<p>(1-Methyl-1H-benzoimidazol-2-yl)-acetonitrile is a nucleophilic compound that reacts with carbanions to form alkyl benzoates. It can also act as an electrophile in the formation of nitroalkenes and amides, as well as an intermediate in the synthesis of phenazines. The potassium salt of this compound is used as a reagent in organic synthesis. (1-Methyl-1H-benzoimidazol-2-yl)-acetonitrile has been shown to react with methylene and aromatize to produce ethyl cyanoacetate, which can be used for the production of malononitrile. This reaction is catalyzed by potassium carbonate and esters.</p>

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<p>Potassium tetracyanoaurate(III) (K[AuCl4]) is a crystalline, intermetallic compound that has been used in the production of coatings, spherical particles, and electrochemical materials. The pentahydrate form has a diameter of 4.8-5.2 Å and a melting point of ~115°C. K[AuCl4] is stable in air and water but reacts with strong acids to form potassium chloride and potassium tetracyanocuprate(II). This substance also has an optimal pH range of 6-7 and an average solubility range of 0.05-0.1g/100mL at 20°C. The microstructure of K[AuCl4] is not well understood because it is difficult to isolate from other compounds during synthesis.</p>

<p>2-Chloro-6-cyanopyrazine is a compound that has been shown to have antimycobacterial activity against Mycobacterium avium. It may also have tuberculostatic activity and be useful for the treatment of tuberculosis. 2-Chloro-6-cyanopyrazine inhibits bacterial growth by binding to DNA, RNA, and protein synthesis in mycobacteria. The antibacterial effect is due to its ability to inhibit amidation and alkylation reactions, as well as its nucleophilic properties. 2-Chloro-6-cyanopyrazine is an acidic compound with a pKa of 3.2, which makes it more soluble in water than hydrophobic compounds such as alkanoic acids.</p>

<p>N-Cyanobenzenecarboximidamide hydrochloride (NCBCH) is an intermediate for the synthesis of azomethine dyes. It can be used to produce azo dyes with a methoxy group at the 3 position and a hydrogen atom at the 4 position. NCBCH is also an excellent substrate for chemical reactions involving fragmentation, extraction, or elimination. NCBCH can be synthesized from methyl ether and benzonitrile in the presence of benzamidine. The product is then treated with methanol to give a tautomeric mixture of benzyl and methyl ether.</p>

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<p>4-(Pyridin-2-yloxy)benzonitrile is a reagent that is used in the synthesis of heterocycles. It is also a useful intermediate for the preparation of highly substituted pyridine derivatives. 4-(Pyridin-2-yloxy)benzonitrile can be used to synthesize complex compounds, such as pharmaceuticals and agricultural chemicals.</p>

<p>Cyanoacetohydrazide is a nucleophilic compound that can react with a variety of molecules, including fatty acids and hydroxy methyl groups. The mechanism of this reaction involves the nucleophilic attack of the cyanide ion on the carbonyl group. This type of reaction has been shown to be reversible and involve the formation of an intermediate hemiacetal, which then attacks another molecule. Cyanoacetohydrazide is used as an antimicrobial agent in some products, such as mouthwashes and toothpaste. It also has anticancer activity.</p>

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<p>Dimethylcyanamide is an organic compound that can be synthesized from cyanide or cyanic acid. Dimethylcyanamide is a colorless liquid with a strong odor. It has been used in the past as a precursor to other compounds, but it has since been replaced by cheaper and more convenient methods. Dimethylcyanamide reacts with primary amines to form nitriles, which are useful intermediates in organic synthesis. In addition, the reaction of dimethylcyanamide with secondary amines leads to the formation of primary amines. The transamination of dimethylamine-N-oxide yields a-dimethylaminopropionitrile as an intermediate product. The elimination reaction mechanism for this process involves the conversion of ammonia into hydroxide ions and hydrogen gas. This reaction produces high yields for both products and does not require high temperatures or pressures.</p>

<p>Potassium tetracyanoplatinate(II)trihydrate (KTP) is a nanomaterial that is made of metal ions, such as ruthenium and copper, and organic molecules. It has the ability to absorb electrons from water, which are then transferred to carbon sources. This process can be used to remove proton in the water, thereby creating an acidic solution. The KTP particles have been shown to produce cavitation when exposed to ultrasound waves or other high-frequency sound waves. Cavitation occurs when bubbles form and rapidly collapse within a liquid. The resulting shockwaves can break down the cell membrane of microorganisms.</p>

<p>3-Cyanopropionic acid methyl ester is a compound that belongs to the class of aliphatic carboxylic acids. It is an intermediate in the production of adiponitrile and acrylonitrile. This compound is used as a feedstock for the manufacture of vinylene, which can be used to produce c1-6 alkyl. 3-Cyanopropionic acid methyl ester can be produced from propylene and hydrogen cyanide in a high salt, activated reaction system. It has been shown that this compound may have metabolic disorders due to its ability to inhibit fatty acid oxidation and increase viscosity. 3-Cyanopropionic acid methyl ester is a colorless liquid at room temperature with a boiling point of 154°C and a molecular weight of 98.14 g/mol.</p>

<p>Ethyl (R)-(-)-4-cyano-3-hydroxybutyrate is an asymmetric synthesis of D-(+)-glyceraldehyde. This compound is an acidic, high cholesterol substrate that binds to disaccharides and has hydroxyl groups. It has been shown to reduce low density lipoprotein levels in the blood by inhibiting the production of cholesterol in the liver. The reaction solution is immobilized on a solid support and is used for kinetic studies. Kinetic measurements were performed at different concentrations of hydrochloric acid and immobilized cells as a function of time. The reaction yield was determined using UV absorbance at 275 nm, which was plotted against time.</p>

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<p>Cyanoguanidine is an antimicrobial agent that inhibits the growth of bacteria by interfering with the synthesis of folic acid. This inhibits the production of DNA and protein, thereby leading to cell death. Cyanoguanidine has been shown to be effective in a model system for blood sampling and has been used as a pharmacological treatment for infectious diseases such as malaria. The optimum concentration for cyanoguanidine is between 5-20 mM, depending on the bacterial species. It can be synthesized from sulfamoyl chloride and dicyandiamide, which are commercially available chemicals. The analytical method for determining the inhibitory effects of cyanoguanidine on bacterial growth is plasma mass spectrometry.</p>

<p>2-Cyanophenothiazine is an aliphatic hydrocarbon that belongs to the class of industrial chemicals. It is used as a reactant in organic synthesis, such as for the production of 2-cyanophenols and 2-phenylbenzimidazole. This compound can be produced by reacting n-hexane with amide or n-dimethylformamide. 2-Cyanophenothiazine has been shown to have mitochondrial biogenesis effects and increase mitochondrial membrane potential in thp-1 cells. It also has biological properties, such as being anti-inflammatory and having antitumor activity.</p>

<p>2-Cyano-5-fluoropyridine is a potential antitubercular agent that has shown penetrability in the central nervous system and activity against Mycobacterium tuberculosis. It is orally active at low doses, and has been shown to be an effective inhibitor of mycobacterial growth and lipid synthesis. In addition, this compound also has antimycobacterial activity against M. avium complex and M. ulcerans, and is a potent inhibitor of β-amyloid aggregation.</p>

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<p>4-Cyanobutanoic acid is a colorless organic solvent that is not soluble in water or polar organic solvents. It can be used for the immobilization of proteins, as well as for the desymmetrization and chlorination of aromatic compounds. One of its most common uses is in biocatalysis, where it acts as a substrate binding agent to help catalyze reactions. 4-Cyanobutanoic acid has also been shown to inhibit the growth of bacteria by acting as an electron acceptor during metabolism. This compound can be degraded through hydrolysis with hydrochloric acid or biodegradation.</p>

<p>2-fluoro-4-iodobenzonitrile is a potent inhibitor of the functions of VEGFR receptors. It inhibits the proliferation and migration of cancer cells by binding to VEGFR receptors, which are tyrosine kinases that regulate cell growth and differentiation. 2-Fluoro-4-iodobenzonitrile has been shown to inhibit angiogenesis, or the formation of new blood vessels, in vitro. This drug also has potent inhibitory activity against tumor growth in vivo. Clinical trials have shown that 2-fluoro-4-iodobenzonitrile can be used to treat various types of cancers, including breast cancer and colon cancer.</p>

<p>Ethyl 2-(3-cyano-4-isobutoxyphenyl)-4-methyl-5-thiazolecarboxylate (ECIT) is a derivative of formyl that has been used as a solvent for industrial and laboratory purposes. ECIT is an amorphous substance with the chemical formula CH3COC6H2CH2COCH=N(C=O)C6H4CN. The compound has been quantified in various solvents, such as n-butyl alcohol and acetonitrile. ECIT is a colorless liquid that boils at 140° C. It has a formyl group and an alkynyl group, which are both reactive groups that can be used to synthesize other compounds. ECIT also contains two stereoisomers: the erythro isomer and the threo isomer. The erythro isomer has the structural formula of CH3COC6H2CH</p>

<p>Alpha-acetylphenylacetonitrile is a synthetic chemical compound that is used as a reagent in the analytical methods of wastewater. It has been shown to be an effective bifunctional agent for the treatment of wastewater, with fluorescence properties that can be used for detection and quantification of cyanide. Alpha-acetylphenylacetonitrile can also be used as a reagent in analytical chemistry techniques, such as gas chromatography and high performance liquid chromatography. This chemical compound has been shown to react with naphthalene to form alpha-naphthol by heating at 190 °C, which can then be used to synthesize phenacyl acetate. The acid catalyst may be either sulfuric acid or hydrochloric acid.</p>

<p>4-Cyano-2-fluorobenzyl bromide is a methyl ester that can be used as a reagent for the synthesis of chiral α-amino acids. It can also be used as an enantioselective methylating agent for the synthesis of γ-secretase inhibitors. The methodology for the convergent synthesis of this compound includes alkylation with glycine followed by an enantioselective hydrolysis, which results in optically pure 4-cyano-2-fluorobenzyl bromide.</p>

<p>Diethyl cyanophosphonate is a compound that is used as a fluorescence probe for amides and pyrazole rings. It binds to the ester form of the amide, which can then be detected with a fluorescence detector. The chemical reaction between diethyl cyanophosphonate and the ester form is reversible, so it can be used as a hypoglycemic agent. Diethyl cyanophosphonate has potent antitumor activity and binds to nerve cells, causing them to become electrically active.</p>

<p>2,4,6-Trimethylbenzonitrile (TMBN) is a reactive unsaturated ketone that reacts with phosphorus pentachloride to form the corresponding chloroform. It is used in nucleophilic substitution reactions and can be hydrolyzed by hydrochloric acid to form an n-oxide. The reaction mechanism of TMBN with phosphorus pentachloride has been studied using molecular modeling and NMR spectroscopy. TMBN can be converted into an oxide, which can react with hydrogen chloride to form the corresponding chloroform. Reaction products include the 2,4,6-trichlorobenzonitrile (TCBN), which is a carcinogen.</p>

<p>Potassium dicyanoargenate is an organic acid that is a precursor to silver nanoparticles. This compound is typically used in the production of cellulose derivatives, and for the activation of polymerization reactions. Potassium dicyanoargenate can also be used to produce insoluble polymers and cationic surfactants by combining it with a metal ion, such as sodium carbonate or hydroxyl groups.</p>

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<p>(Triphenylphosphoranylidene)acetonitrile is a phosphorane that has been shown to have an inhibitory effect on the inflammatory response in animal models of bowel disease. It also has been shown to be effective in treating inflammatory diseases such as arthritis and multiple sclerosis. This drug binds to leukotriene D4, an inflammatory mediator, and inhibits its production by blocking the enzyme 5-lipoxygenase. The compound also has been shown to possess anti-inflammatory properties due to its inhibition of prostaglandin synthesis. (Triphenylphosphoranylidene)acetonitrile is used as a pharmaceutical preparation for the treatment of bowel disease, inflammatory diseases, and other conditions.</p>

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

<p>Ethyl cyanoformate is a reactive compound that is used in organic synthesis. It has been shown to cause muscle cell proliferation and inhibit the production of gamma-aminobutyric acid, which is responsible for regulating neurotransmitter release. Ethyl cyanoformate also has antimicrobial properties due to its ability to form an oxygenated n-oxide tautomer. The reaction mechanism of ethyl cyanoformate involves the formation of a covalent bond with the sulfhydryl group on the enzyme gamma-aminobutyric acid receptor. This prevents the binding of GABA, inhibiting nerve impulses and reducing inflammation in the bowel.</p>

<p>Bromodichloroacetonitrile (BCN) is a chemical with disinfectant properties. It is used in wastewater treatment, as it is able to destroy bacteria and viruses. BCN also has been shown to be effective against the Covid-19 pandemic. BCN can be used as an analytical reagent for the analysis of chloride ions in deionized water. The carcinogenic potential of BCN in humans is unknown, but it has been shown to cause bladder cancer in rats.</p>

<p>5-Cyanopyridine-2-carboxylic acid is a small molecule that has been found to have significant biological activity in a number of different areas, including neurotherapeutics. It is the result of a scalable synthesis and is soluble in water. The molecule has two chiral centers and can exist as four different stereoisomers (enantiomers). In vitro studies show that 5-cyanopyridine-2-carboxylic acid inhibits fatty acid uptake by blocking the proton pump, which transports lipids into cells. This compound also binds to the cytosolic protein pyrazine 2-carboxylic acid receptor 1 (PYZR1), which may provide an explanation for its effects on fatty acid uptake.</p>

<p>3-Cyanoethylbenzoic acid is an anthropogenic compound that is produced by the Friedel-Crafts reaction between benzoyl chloride and acrylonitrile in the presence of a base. 3-Cyanoethylbenzoic acid is used as a solvent for chromatographic methods, such as gradient elution, ion exchange, and reversed phase. 3-Cyanoethylbenzoic acid has been used to determine the optical purity of benzoate salts and amides. This compound can be taken orally in solid oral dosage form or enterically in liquid oral dosage form. 3-Cyanoethylbenzoic acid interacts with other drugs that are metabolized by CYP3A4, such as erythromycin, to produce an active metabolite (N-desmethyldesipramide).</p>

<p>2,4,5-Trimethoxybenzylamine is a synthetic compound that can be used as a precursor to the synthesis of other chemicals. It is prepared by reacting phenol with deuterium gas in a process called amination. This reaction is followed by reductive quaternization with cyanide. 2,4,5-Trimethoxybenzylamine is often used as an intermediate for the synthesis of drugs such as tamoxifen and clonidine.</p>

<p>Iminodiacetonitrile is a chemical compound that is used in wastewater treatment. It is a nitrite-oxidizing agent that reacts with nitrite ion to form nitric acid, which can be then used to oxidize hexamethylenetetramine and iminodiacetic acid to produce ammonia and cyanide ions. Iminodiacetonitrile has an optimum pH of 7.5, so it will not react at higher or lower pH levels. This reaction occurs in the presence of hydroxide solution, hydrochloric acid, and inorganic acids such as sulfuric acid or phosphoric acid. The reaction mechanism for this process is shown below: C6H11N2O2 + HNO3 → C6H11N2O4 + H+ + NO2- C6H11N2O4 → NH3 + HCN</p>

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<p>2,3-(Dimethoxyphenyl)acetonitrile is a chemical intermediate that is used in the synthesis of pharmaceuticals and specialty chemicals. It can be used as a reaction component and reagent for the synthesis of other chemicals. This compound has a high quality and is also a versatile building block for complex compounds. 2,3-(Dimethoxyphenyl)acetonitrile has been shown to be useful in the production of fine chemicals such as pharmaceuticals, agrochemicals, and dyes. The CAS number for this compound is 4468-57-9.</p>

<p>3-Cyano-2-methylphenylboronic acid is a high quality compound that can be used as a reagent, intermediate, or building block in the synthesis of complex compounds. This chemical is also useful as a speciality chemical and research chemical. 3-Cyano-2-methylphenylboronic acid has versatile uses in organic synthesis due to its versatility in reactions and building blocks.</p>

<p>N-(4-Chlorophenyl)-2-cyanoacetamide is a pyridine compound that can be synthesized from chloroacetonitrile and acetamide. It has been shown to react with an active methylene group in benzene or pyridine to produce a heterocycle. This reaction is reversible and can be used as a preparative method for the synthesis of heterocycles. The 1,3-dipolar cycloaddition of N-(4-chlorophenyl)-2-cyanoacetamide with nitro groups in nitrobenzene produces the corresponding 2-nitropyridines, which are important intermediates in the synthesis of other heterocycles. N-(4-Chlorophenyl)-2-cyanoacetamide has been used as an efficient method for the preparation of nitrogen nucleophiles that are useful for catalysis.</p>

<p>Imidazol-1-ylacetonitrile is a synthetic compound that belongs to the class of ethyl methanesulfonates. It has been shown to be an effective antifungal drug against Candida spp. and Aspergillus spp., with a minimum inhibitory concentration (MIC) of 0.5 μM in vitro. Imidazol-1-ylacetonitrile has also been shown to have anti-inflammatory properties and was able to reduce bone resorption in mice, as well as inhibit the production of osteoclasts in vitro by inhibiting the activity of cathepsin K, which is an enzyme involved in bone resorption. This compound may be used for the treatment of metabolic disorders such as diabetes mellitus type 2 and hyperglycemia, since it inhibits glucose uptake by decreasing the expression of GLUT4 at the cell membrane level.</p>

<p>p-(Methylthio)phenylacetonitrile (p-MTPA) is a synthetic analgesic that belongs to the group of benzyl derivatives. It has analgesic, antiinflammatory and antipyretic properties. p-MTPA is used in organic synthesis as a hydrolysis reagent for benzyl halides. The drug has been shown to be an inhibitor of cyclooxygenase-2 (COX-2) and exerts its effects by decreasing prostaglandin production. P-MTPA is also decarboxylated to produce benzoic acid and phenylacetic acid, which have acidic properties.</p>

<p>3,5-Bis(trifluoromethyl)phenylacetonitrile (3,5-BTFAPN) is a compound that has anticancer activity. It can be used to treat cancer by inhibiting the growth of cancer cells. 3,5-BTFAPN has been shown to be effective against some human cancer cell lines in vitro and in vivo. The drug was found to have cytotoxic effects by inducing apoptosis through changes in mitochondrial membrane potential and cytochrome c release. 3,5-BTFAPN also binds to DNA and forms adducts with guanine residues, which may explain its anticancer activity.</p>

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<p>2-[4-(2-Cyanoethylthio)methyl]thiazolyl guanidine (HCTZ) is a histamine H2 receptor antagonist that belongs to the class of synthetic compounds. It is an effective anti-histamine and has been shown to inhibit acid secretion in the stomach in response to histamine. HCTZ also inhibits the release of gastric acid by blocking the action of histamine on the H2 receptor of parietal cells, which are located in the lining of the stomach. This drug is also used for treating reflux esophagitis and gastroesophageal reflux disease. Other uses include as a proton pump inhibitor for treatment of peptic ulcers, and as an adjunct therapy for ulcerative colitis. The following product details are about a company that sells organic food products:</p>

<p>4-Isopropylphenylacetonitrile is a nicotinic receptor agonist. It has high affinity for the nicotinic acid receptor, and potentiates the response to other nicotinic receptor agonists. 4-Isopropylphenylacetonitrile was discovered by screening for acid binding compounds and allosteric potentiators of the nicotinic acid receptor. This compound binds to the ion channel in the central nervous system, which leads to increased neuronal excitability and decreased pain sensation. 4-Isopropylphenylacetonitrile also displays antiinflammatory properties due to its ability to inhibit prostaglandin synthesis.</p>

<p>3-Fluoro-4-hydroxybenzonitrile is a compound with an acidic ph and a strain that is dispersive, desorptive, and polyacrylamide gel. It is a colorless liquid at room temperature. 3-Fluoro-4-hydroxybenzonitrile has been shown to react with dodecyl inorganic base and hydrochloric acid to produce 3-fluoroaniline. The localization of the reaction yield is on hydrotalcite activated by fluorine. This chemical has been shown to react at temperatures between 0°C and 140°C.</p>

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<p>Candesartan is a selective angiotensin II receptor antagonist that inhibits the binding of angiotensin II to its receptors, which in turn decreases the activity of angiotensin-converting enzyme. Candesartan cilexetil is an ester prodrug that has been shown to be effective in the treatment of high blood pressure. In the crystalline form, candesartan cilexetil is a white powder with a melting point of 130–135 °C and a solubility in water of &gt;1 g/L. The molecular weight of candesartan cilexetil is 393.8 g/mol and it has a molecular formula C17H21NO2S. The chemical structure consists of two benzimidazole rings coupled together through an ethyl-2-ethoxy linker and attached to a carboxylate group on one end and an amide group on the other</p>

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<p>N-Allyl-n-(2-chloro-5-cyanophenyl)acetamide is a fine chemical that is used as a building block in the synthesis of other compounds. It is also used in research and as a reagent or speciality chemical. N-Allyl-n-(2-chloro-5-cyanophenyl)acetamide has been shown to be an excellent intermediate for complex organic reactions, such as coupling reactions with amines, alcohols, and thiols. In addition, this compound can be used to form new scaffolds for biological studies.</p>

<p>Ethyl 2,3-dicyanopropionate is a white crystalline solid that is soluble in organic solvents. It has the molecular formula CHClNOS and the molecular weight of 138.1 g/mol. This compound has a melting point of 92 °C and can be purchased as a mixture of cis and trans isomers. The cis form melts at 93 °C and the trans form melts at 88 °C. Ethyl 2,3-dicyanopropionate is synthesized from chlorobenzene by dehydrating it with hydrochloric acid in an organic solvent. It can also be prepared by reacting ethyl cyanoacetate with ammonia in an inert atmosphere. Impurities may include chloride, sulfoxide, or imine.</p>

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<p>1-Cyano-4-(dimethylamino)benzene is a molecule that has been shown to inhibit the growth of hamster v79 cells. It also inhibits the synthesis of DNA and RNA. The binding constants for this molecule have been determined to be 1.0 x 10^9 M^-1, with an n-octanol/water partition coefficient (log P) of 5.5. This molecule is soluble in nonpolar solvents and may be used as a model system for hydrogen bonding interactions or reaction mechanisms in organic chemistry. This compound contains a deuterium isotope and can be used to study the effects of hydrogen bonding on reactions in organic chemistry at high temperatures, with the use of preparative hplc.</p>

<p>Please enquire for more information about N-2-Cyanoethyl-Val-Leu-anilide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Bromo-3-cyanoanisole is a potent inhibitor of the tyrosine kinase receptor. The functional theory behind this drug's mechanism of action is that it binds to the ATP binding site of the receptor and blocks ATP from binding, preventing downstream signaling. 4-Bromo-3-cyanoanisole has been shown to be an effective inhibitor of cancer cell proliferation. This drug has also been shown to inhibit microtubule assembly and disrupt cellular function by inhibiting protein synthesis.</p>

<p>3-Cyanopropanoic acid is a reactive compound that forms a complex with palladium. It is produced by the reaction of acrylonitrile and chloride in the presence of a base such as sodium hydroxide. The reaction mechanism is shown below:</p>

<p>Cyanoac-Phe-Phe-OH is a hydrolytic enzyme that irreversibly inactivates the ACE enzyme. It acts as an inhibitor of angiotensin-converting enzyme and inhibits the conversion of angiotensin I to angiotensin II, which is involved in blood pressure regulation. Cyanoac-Phe-Phe-OH has been shown to be more potent than captopril, another ACE inhibitor. It also has a longer half life and greater selectivity for ACE over other serine proteases.</p>

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

<p>Biphenylacetonitrile is an organic compound that belongs to the group of reactive functional groups and is used as a reagent in organic synthesis. It has been shown to inhibit the growth of cancer cells, likely due to its ability to react with sulfamates. Biphenylacetonitrile inhibits the production of the inflammatory mediator nitric oxide by reacting with trifluoroacetic acid, which may be useful for treating inflammatory diseases such as endometriosis. This drug also has an inhibitory effect on fatty acid metabolism and can thus be used for treating diabetes patients.</p>

<p>2-Chlorobenzonitrile is a white solid that is soluble in organic solvents. It is an aryl halide and has a chemical structure of C6ClCN. 2-Chlorobenzonitrile is used as a raw material for the production of dyes and pharmaceuticals. This compound reacts with hydrochloric acid to form 4-chlorobenzonitrile, which can be used in the synthesis of other chemicals. 2-Chlorobenzonitrile can also react with n-dimethyl formamide in an optimal reaction solution to form 4-chlorobenzonitrile. The FTIR spectroscopy on this compound shows that it has a chloride group at 795 cm−1. The optimum reaction temperature for this compound is between 100 and 120 °C, but it will react with inorganic acids such as sulfuric acid or phosphoric acid at higher temperatures. Synthesis of this compound can be done by reacting</p>

<p>2-Cyano-3,4,5,6-tetrachloropyridine is a genotoxic compound that is used for the preparation of picolinic acid. It has been shown to induce DNA damage and cytotoxicity in vitro. The reaction products of this compound have also been found to be genotoxic in vitro and in vivo. This chemical has been shown to inhibit the growth of cells in culture as well as cause cell death by releasing hydrogen chloride gas. 2-Cyano-3,4,5,6-tetrachloropyridine is a potent mutagen and carcinogen that can be activated by fluorine or chlorine compounds. This chemical can also form chlorinated derivatives with chlorine. 2-Cyano-3,4,5,6-tetrachloropyridine reacts with phosphorus pentachloride to produce hydrogen chloride gas and other reaction products such as chloride (Cl) or sublimed (P</p>

<p>1,6-Bis(cyano-guanidino)hexane is a bactericidal agent that can be used to remove bacteria from water. The compound has been shown to have a bactericidal activity against Gram-positive and Gram-negative bacteria in concentrations of 100 mg/L and 200 mg/L, respectively. 1,6-Bis(cyano-guanidino)hexane has also been shown to be effective against industrial strains of Bacillus subtilis and Pseudomonas aeruginosa in concentrations of 200 mg/L. This compound is soluble in organic solvents but insoluble in deionized water. It has a viscosity of 30000 cP at 20°C and an anion charge of -1.</p>

<p>Phycocyanobilin is a chromophore found in blue-green algae and cyanobacteria. It is a component of the holoprotein phycocyanin and aids in the harvesting of light energy. This biliverdin derivative is converted to phycocyanorubin by biliverdin reductase in mammalian cells. The addition of phycocyanobilin to human cells leads to potent inhibition of NADPH oxidase. It also binds to human serum albumin (HSA). Structurally, Phycocyanin shares many similarities to bilirubin and biliverdin.</p>

<p>Please enquire for more information about 3'-[2- Cyanoethyl N, N- bis(1- methylethyl) phosphoramidite]-5'- O- [bis(4- methoxyphenyl) phenylmethyl] - 2'- O- methyl- N- [2- [4- (1- methylethyl) phenoxy] acetyl] -guanosine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,6-Dimethoxy-4-hydroxybenzylamine is a fine chemical that is used as a versatile building block for the synthesis of complex compounds. It is also used as a reagent and reaction component in various chemical reactions. CAS No. 130632-98-3.</p>

<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.</p>