Cyano-, Nitrile-

<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 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 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-(3-Chloro-4-fluorophenyl)-2-cyanoacetamide (cas# 219529-31-4) is a compound useful in organic synthesis.<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>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-(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 Ethyl Cyanoformate (cas# 623-49-4) is a compound useful in organic synthesis.<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 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>