Ciano-, nitrilo-

<p>Please enquire for more information about Isocyanomethyl resin (200-400 mesh) including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>

<p>Please enquire for more information about 1-Boc-5-Cyano-3-hydroxymethylindole including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>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>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>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>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>

<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>

<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>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>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>

<p>Please enquire for more information about 2,2'-(Perchloro-1,2-phenylene)diacetonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>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>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>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>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>

<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>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>