Cyano-, Nitrile-

<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 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>Please enquire for more information about 2-Chloro-N-(3-chloro-4-cyanophenyl)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>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>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>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 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>Applications p-Cyanobenzoic Acid Trimer is used in the synthetic preparation of Terbium Triazinetribenzoate Formate Metal Organic Framework (MOF).<br>References Han, Y., et al.: J. Mater. Chem. A Mater. Energy Sustain., 3, 24525 (2015)<br></p>

<p>Applications Methyl Isocyanoacetate, is used in the Cu-catalyzed, diastereoselective synthesis of oxazolines (O846550).<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 Ideguchi, T., et al.: J. American Chem. Soc., 135, 12568 (2013);<br></p>

<p>Applications 4-Biphenylacetonitrile is a useful synthetic intermediate. It was used to study the adsorption orientation of the biphenyl derivatives on the Au colloidal surfaces with α-cyclodextrins. 4-Biphenylacetonitrile on condensation reaction with ethyl phenyl propiolate yields biphenyl derivatives of acetylenic β-ketocyanide.<br>References Lee, J., et al.: Bull. Korean. Chem. Soc., 30, 1637 (2009); Al-Jallo, H., et al.: J. Chem. Eng. Data, 17, 513, (1972)<br></p>

<p>Applications Methyl 2-cyanobenzoate<br></p>

<p>Applications Pentachlorophenyl Cyanoacetate is an intermediate used in the synthesis of Cefacetrile (C231500), which is a cephalosporin antibiotic. Antibacterial.<br>References Dajan, A., et al.: Vet. Microbiol., 35, 213 (1993), Becker, M., et al.: Anal. Chim. Acta, 520, 19 (2004), El-Shaboury, S., et al.: J. Pharm. Biomed. Anal., 45, 1 (2007),<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>