Ciano-, Nitrilo-

<p>Please enquire for more information about 4-Isopropylbenzenesulphonylacetonitrile 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 (4-Formylphenoxy)acetonitrile 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 ethyl 2-cyano-3-[3-(trifluoromethyl)phenyl]acrylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(4-Chlorobenzenesulphonyl)acetonitrile is a reactive chemical that is synthesized from chloroform and acetonitrile. It can be used to synthesize various medicines such as analgesics, muscle relaxants, and x-ray contrast agents. 2-(4-Chlorobenzenesulphonyl)acetonitrile has minimal effects on the human body and is not known to cause any major health problems. It is metabolized in the liver by oxidation of the methyl group to form 4-chlorobenzene sulfonic acid, which is excreted through urine. The chlorine atom in this molecule has a trigonal bipyramidal geometry with a bond length of 1.82 Å, which can be seen in x-ray crystallography studies.</p>

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

<p>2-(Dicyanomethylene)indan-1,3-dione is a zwitterion that can be used as an acceptor in organic synthesis. It reacts with nucleophiles (e.g., amines) to form the corresponding adducts and is reversibly hydrolyzed by water or alkali. 2-(Dicyanomethylene)indan-1,3-dione is also known for its ability to undergo nucleophilic attack of the carbonyl group and react with anilines to form the corresponding azine derivatives. This molecule has been shown to be a good candidate for use in uv irradiation due to its high absorption coefficient at 260 nm.</p>

<p>Please enquire for more information about 4-Bromobenzenesulphonylacetonitrile 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 2,4-Dichlorobenzenesulphonylacetonitrile 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 2-((4-(tert-butyl)phenyl)sulfonyl)acetonitrile 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 N-(4-Cyanophenyl)-2-chloropropanamide 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 2-Chloro-N-(4-(cyanomethyl)phenyl)propanamide 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 4-(Trifluoromethoxy)benzenesulphonylacetonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(Aminomethylene)phenylsulphonyl acetonitrile is an allylating agent. It reacts with hydrochloric acid to form allyl isothiocyanate, which can be used for the synthesis of thiazoline derivatives. 2-(Aminomethylene)phenylsulphonyl acetonitrile is a reagent that has been used in multicenter trials to study the effects of allylation on cancerous cells.</p>

<p>Applications (2-Isocyanoethyl)-benzene is a useful synthetic intermediate. It is a reagent used in Ugi reactions to synthesize various compounds such as tetrazole and bisamide.<br>References Zhao, T., et al.: Org. Lett., 15, 639 (2013); Brockmeyer, F., et al.: Helv. Chim. Acta., 95, 1857 (2012)<br></p>

<p>Stability Air Sensitive, Light Sensitive<br>Applications 2-Amino-4-cyano-phenol<br></p>

<p>Applications A Wittig reagent.<br>References Laine, D., et al.: J. Med. Chem., 52, 5241 (2009), Nakao, A., et al.: Bioorg. Med. Chem. Lett., 19, 4607 (2009), Arakawa, Y., et al.: Chem. Pharm. Bull., 57, 167 (2009),<br></p>