CAS 95092-10-7

Benzeneacetamide, N-methoxy-N-methyl-

Description:

Benzeneacetamide, N-methoxy-N-methyl- is an organic compound characterized by its amide functional group, which is derived from benzeneacetic acid. This compound features a methoxy group (-OCH3) and a methyl group (-CH3) attached to the nitrogen atom of the amide, contributing to its unique chemical properties. It typically appears as a colorless to pale yellow liquid or solid, depending on its physical state at room temperature. The presence of the aromatic benzene ring imparts stability and hydrophobic characteristics, while the methoxy and methyl substituents can influence its solubility and reactivity. This compound may exhibit biological activity, making it of interest in pharmaceutical research. Its molecular structure allows for potential interactions with various biological targets, which could be explored for therapeutic applications. As with many organic compounds, safety data should be consulted to understand its handling and potential hazards.

Formula: C₁₀H₁₃NO₂

Synonyms:

• N-methoxy-N-methylbenzeneacetamide
• Benzeneacetamide, N-methoxy-N-methyl-
• N-Methoxy-N-Methyl-2-phenylacetaMide

Benzeneacetamide, N-​methoxy-​N-​methyl-

CAS: 95092-10-7

Formula: C₁₀H₁₃NO₂

Purity: 95%

Color and Shape: Liquid

Molecular weight: 179.2157

Ref: IN-DA005TF7

N-methoxy-N-methyl-2-phenylacetamide

CAS: 95092-10-7

N-methoxy-N-methyl-2-phenylacetamide

Purity: 99%

Molecular weight: 179.22g/mol

Ref: 54-OR79447

N-methoxy-N-methyl-2-phenylacetamide

CAS: 95092-10-7

Formula: C₁₀H₁₃NO₂

Purity: 98%

Color and Shape: Liquid

Molecular weight: 179.219

Ref: 10-F523367

N-Methoxy-N-methyl-2-phenylacetamide

CAS: 95092-10-7

N-Methoxy-N-methyl-2-phenylacetamide is a synthetic, nucleophilic alkylating agent that is used in the treatment of cancer. It inhibits the growth of cells by attacking the nucleophiles such as thiols and amino groups in proteins, DNA, RNA, and other cellular molecules. N-Methoxy-N-methyl-2-phenylacetamide has been shown to be effective against chlorido and prenylated compounds. The drug has also been shown to have anticancer activity against several types of cancer cells including leukemia cells. This drug binds to DNA at the five membered ring positions where it forms a stable covalent bond with the phosphate group on the sugar moiety of DNA, preventing replication and transcription.

Formula: C₁₀H₁₃NO₂

Purity: Min. 95%

Molecular weight: 179.22 g/mol

Ref: 3D-VDA09210