Cyano-, Nitrile-

<p>Applications Ethyl Cyanoformate (cas# 623-49-4) is a compound useful in organic synthesis.<br></p>

<p>Applications Phthalodinitrile monomers can be polymerized thermally in the presence of small amounts of curing agents into thermosetting polymers. Phthalodinitrile is a precursor to phthalocyanine which is used as a dye or pigment.<br>References Sastri, S. B. and Keller, T. M.: J. Polym. Sci. A Polym. Chem., 36, 1885-1890(1998), Löbbert, G. Phthalocyanines. In Ullmann's Encyclopedia of Industrial Chemistry, (Ed.)., (2000).<br></p>

<p>Applications Methyl cyanoformate is a reagent that is used in the preparation of XEN907, which is a spiro-oxindole blocker of Nav1.7 for the treatment of pain.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Chowdhury, S., et al.: Bioorg. Med. Chem. Lett., 21, 3676 (2011);<br></p>

<p>Applications 4-Cyanophenol is used in a study to assess chemical uptake into human stratum corneum.<br>References Stinchcomb, A.L., et. al.: Pharm. Res., 16, 1288 (1999)<br></p>

<p>Applications Ethyl 2-Cyanopropanoate is a building block used in many organic reactions such as the preparation of highly substituted benzenes.<br>References Zhang, X., et. al.: Organic Lett., 13, 5024 (2011)<br></p>

<p>Applications N-(3-Chloro-4-fluorophenyl)-2-cyanoacetamide (cas# 219529-31-4) is a compound useful in organic synthesis.<br></p>

<p>Applications 2-Cyano-N-((furan-2-ylmethyl)carbamoyl)acetamide is an intermediate in the synthesis of novel 1- and 8-substituted-3-furfuryl xanthines as adenosine receptor antagonists.<br>References Balo, M. C., et al.: Bioorg. Med. Chem., 17, 6755 (2009);<br></p>

<p>Applications N-(β-Cyanoethyl)-N-(ethoxycarbonylethyl)benzylamine is a compound useful in organic synthesis.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br></p>

<p>Applications Tetrakis(acetonitrile)palladium Bis(tetrafluoroborate) is used to prepare an α-Diimine-transition metal complex, which is used as a catalyst for polymerization of olefins. It is also a catalyst used in cross coupling reaction for C-C, C-O, and C-N bond formation.<br>References Feldman, J., et al.: Organometallics, 16, 1514 (1997); Johnson, L., et al.: PCT Int. Appl., WO 9623010 A2 19960801 (1996); Poppenbery, J., et al.: Surface Sci., 2011; Pijnenburg, N., et al.: Dalton Transactions, 40, 8896 (2011); Kilpin, K., et al.: Inorg. Chem., 50, 6334 (2011)<br></p>

<p>Applications Methyl Cyanoacetate is often used as a nucleophile in the electrochemical oxidation of catechols. Methyl Cyanoacetate is also a reagent in the synthesis of Methyl 2-Amino-4-trifluoromethylthiophene-3-carboxylate (M287290); a compound used in the synthesis of DPP-IV inhibitors for treating type 2 diabetes.<br>References Rafiee, M., et al.: J. Electroanal. Chem., 626, 36 (2009); Deng, J., et al.: Eur. J. Med. Chem., 46, 71 (2010)<br></p>

<p>2-Chloro-5-methylbenzonitrile (2C5MB) is a versatile building block that is used in the production of fine chemicals, specialty chemicals, and pharmaceuticals. It is also used as a reagent for organic synthesis and as a speciality chemical. 2C5MB can be used in the synthesis of various complex compounds and research chemicals. The compound has been shown to have high reactivity and has been used as a reaction component or scaffold for the synthesis of other products.</p>

<p>2-Cyanopyridine is a chelate ligand that is structurally related to picolinic acid. It binds to the active site of IDO1 and prevents the enzyme from converting tryptophan into kynurenine. This leads to an increase in tryptophan levels, which can then be used for protein synthesis. 2-Cyanopyridine has been shown to have antimicrobial activity against Gram-positive bacteria in vitro and in vivo. It also inhibits the growth of Gram-negative bacteria, yeast, and fungi by binding to the iron atom of their heme molecules. 2-Cyanopyridine has shown potential as a pharmacological agent or as a biochemical probe for transfer reactions.</p>

<p>2-Cyanobenzylamine hydrochloride is a chemical building block and intermediate that can be used in the synthesis of many different compounds. It is also a useful reagent for reactions involving nitro compounds. 2-Cyanobenzylamine hydrochloride is a fine chemical that is registered with the Chemical Abstract Service (CAS No. 1134529-25-1). It has been identified as a versatile building block and useful intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic chemicals.</p>

<p>a-Cyanocinnamic acid is a 3-hydroxycinnamic acid that can be found in coffee. It has been shown to inhibit the growth of colorectal adenocarcinoma cells and other cancer cells by binding to an inhibitor site on fatty acid synthesis enzymes, such as pyruvate carboxylase, hydroxylase, and acetyl-CoA carboxylase. This inhibition leads to decreased levels of fatty acids and increased levels of pyruvate and hydrogen peroxide, which inhibits cell proliferation. In addition, a-cyanocinnamic acid has been shown to have a hypoxic tumor selectivity index of 10.7%, which means it selectively targets tumors with low oxygen levels.</p>

<p>N-Cyanopyrrolidine is a compound that targets enzymes, such as histone deacetylases (HDACs) and protein kinase C. It is a chemical ionization reagent that reacts with hydroxyl groups on the target molecule. This leads to the formation of covalent bonds between the target and the reagent, which results in an irreversible reaction. N-Cyanopyrrolidine has been shown to have antidiabetic effects in diabetic patients and hiv infection by decreasing levels of glucose in the blood. It also inhibits cancer cell growth by inhibiting dpp-IV, which is an enzyme that causes cancer cells to proliferate.</p>

<p>3-Cyanomethylbenzoic acid methyl ester is a synthetic chemical compound that is used as an intermediate in the production of other chemicals. It is a chlorination agent that reacts with toluene and methanol in the presence of chlorine to produce 3-chloromethylbenzoic acid methyl ester. This reaction also produces a byproduct called sulphone, which can be converted into acylation reagents for use in organic synthesis. The chloride ion can be used for cyanation reactions, which are useful for producing dyes or pharmaceuticals.</p>