CAS 39581-30-1
:Acetamide, 2-cyano-N-methyl-N-phenyl-
Description:
Acetamide, 2-cyano-N-methyl-N-phenyl- is an organic compound characterized by its amide functional group, which features a carbonyl group (C=O) directly bonded to a nitrogen atom (N). This compound contains a cyano group (-C≡N) and is substituted with a methyl group and a phenyl group, contributing to its unique chemical properties. It is typically a white to off-white solid and is soluble in polar solvents due to the presence of the amide group. The presence of the cyano group enhances its reactivity, making it useful in various chemical syntheses and applications, including pharmaceuticals and agrochemicals. The compound may exhibit moderate toxicity, and appropriate safety measures should be taken when handling it. Its molecular structure allows for potential interactions with biological systems, which can be explored for medicinal chemistry applications. As with many organic compounds, its stability and reactivity can be influenced by environmental conditions such as temperature and pH.
Formula:C10H10N2O
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Found 3 products.
2-Cyano-N-methyl-n-phenylacetamide
CAS:Formula:C10H10N2OPurity:95+%Color and Shape:SolidMolecular weight:174.2032-Cyano-N-methyl-N-phenylacetamide
CAS:<p>2-Cyano-N-methyl-N-phenylacetamide is a diazo compound that is used as a ligand for the β-lactams. It can be prepared by reacting methylcyanamide with phenylacetic acid in the presence of nitrous acid. 2-Cyano-N-methyl-N-phenylacetamide reacts with carbonyl groups to form an oxime, which can be hydrolyzed to produce an amine. This reaction occurs intramolecularly and catalysed by copper or silver salts. The houben–hoesch reaction of 2,4,6,8 tetramethylpiperidine with 2-cyano N -methyl N -phenyl acetamide yields the piperidine derivative 1-(2 cyanoethyl)-2-(2 methoxyethoxy)ethylamine.</p>Formula:C10H10N2OPurity:Min. 95%Molecular weight:174.2 g/mol
