CAS 7463-32-3

N-(5-Chloro-2-methoxyphenyl)acetamide

Description:

N-(5-Chloro-2-methoxyphenyl)acetamide, with the CAS number 7463-32-3, is an organic compound characterized by its acetamide functional group attached to a substituted aromatic ring. The presence of a chloro group and a methoxy group on the phenyl ring contributes to its unique chemical properties, including potential reactivity and solubility characteristics. This compound typically appears as a solid at room temperature and may exhibit moderate to high stability under standard conditions. Its molecular structure suggests that it may participate in various chemical reactions, such as nucleophilic substitutions or acylation reactions, due to the presence of the acetamide moiety. Additionally, the chloro and methoxy substituents can influence the compound's electronic properties, potentially affecting its biological activity and interactions with other molecules. As with many organic compounds, safety precautions should be taken when handling N-(5-Chloro-2-methoxyphenyl)acetamide, as it may pose health risks or environmental hazards.

Formula: C₉H₁₀ClNO₂

InChI: InChI=1S/C9H10ClNO2/c1-6(12)11-8-5-7(10)3-4-9(8)13-2/h3-5H,1-2H3,(H,11,12)

InChI key: InChIKey=WKZLKZPMUWYXTK-UHFFFAOYSA-N

SMILES: N(C(C)=O)C1=C(OC)C=CC(Cl)=C1

Synonyms:

• o-Acetanisidide, 5′-chloro-
• 2-Acetamido-4-chloroanisole
• Acetamide, N-(5-chloro-2-methoxyphenyl)-
• N-(5-Chloro-2-methoxyphenyl)acetamide
• acetamide, N-(5-chloro-2-methoxyphenyl)-
• N-(5-Chloro-2-methoxyphenyl)acetamide
• 5′-Chloro-2′-methoxyacetanilide
• N1-(5-chloro-2-methoxyphenyl)acetamide