35684-24-3

Basic information

• Product Name: N-(4-butylphenyl)-4-methoxybenzamide
• Synonyms: N-(4-butylphenyl)-4-methoxybenzamide
• CAS NO: 35684-24-3
• Molecular Formula: C₁₈H₂₁NO₂
• Molecular Weight: 283.36484
• Mol File: 35684-24-3.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(4-butylphenyl)-4-methoxybenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-butylphenyl)-4-methoxybenzamide(35684-24-3)
• EPA Substance Registry System: N-(4-butylphenyl)-4-methoxybenzamide(35684-24-3)

Safety Data

• Hazardous Substances Data: 35684-24-3(Hazardous Substances Data)

Upstream product

• 104-13-2 4-Butylaniline 
• 100-09-4 4-methoxybenzoic acid 
• 100-07-2 4-methoxy-benzoyl chloride 

Relevant articles and documents

Base-Promoted Amidation and Esterification of Imidazolium Salts via Acyl C-C bond Cleavage: Access to Aromatic Amides and Esters

Imidazolium salts have been effectively employed as suitable acyl transfer agents in amidation and esterification in organic synthesis. The weak acyl C(O)-C imidazolium bond was exploited to generate acyl electrophiles, which further react with amines and alcohols to afford amides and esters. The broad substrate scope of anilines and benzylic amines and base-promoted conditions are the benefits of this route. Interestingly, phenol, benzylic alcohols, and a biologically active alcohol can also be subjected to esterification under the optimized conditions.

Combination of the topliss approach with the Free-Wilson analysis in the study of antimycobacterial activity of 4-alkylthiobenzanilides

On the basis of a preliminary study of the antimycobacterial activity of thiobenzanilides, a group of 4′-isopropyl- and 4′-butylthiobenzanilides have been synthesized and tested against Mycobacterium tuberculosis, Mycobacterium kansasii, Mycobacterium avi