CAS 6876-65-9
:Benzeneacetamide, N-(4-methylphenyl)-
Description:
Benzeneacetamide, N-(4-methylphenyl)-, also known as p-tolylacetamide, is an organic compound characterized by its amide functional group attached to a benzene ring. It features a benzene ring substituted with a methyl group at the para position relative to the acetamide group. This compound typically appears as a white to off-white crystalline solid and is soluble in organic solvents such as ethanol and acetone, but has limited solubility in water due to its hydrophobic aromatic structure. The presence of the methyl group enhances its lipophilicity, which can influence its biological activity and interactions. Benzeneacetamide derivatives are often studied for their potential pharmacological properties, including analgesic and anti-inflammatory effects. As with many aromatic amides, it may exhibit moderate toxicity, and appropriate safety measures should be taken when handling it in laboratory settings. Its chemical behavior can be influenced by the presence of substituents, making it a subject of interest in synthetic organic chemistry and medicinal chemistry research.
Formula:C15H15NO
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Found 2 products.
N-(4-Methylphenyl)-2-phenylacetamide
CAS:<p>2-Phenylacetamide is a solvent that can be used as a component in alkylation reactions. It is commonly used as a component of chlorinated solvents and has been shown to catalyze the reaction with benzyl chloride. 2-Phenylacetamide can be used to produce solar cells by sensitizing the surface of silicon wafers with this solvent. Researchers have also studied the alkylation reaction of phenylacetamide with methyl iodide and benzyl chloride, which can be carried out at room temperature and does not require any catalyst. This reaction was found to proceed well under gas chromatographic conditions.</p>Formula:C15H15NOPurity:Min. 95%Molecular weight:225.29 g/mol
