200278-95-1

Basic information

• Product Name: methyl 4-[(2-methylbenzoyl)amino]benzoate
• Synonyms: methyl 4-[(2-methylbenzoyl)amino]benzoate;methyl 4-{[(2-methylphenyl)carbonyl]amino}benzoate
• CAS NO: 200278-95-1
• Molecular Formula: C₁₆H₁₅NO₃
• Molecular Weight: 269.2952
• Mol File: 200278-95-1.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: methyl 4-[(2-methylbenzoyl)amino]benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 4-[(2-methylbenzoyl)amino]benzoate(200278-95-1)
• EPA Substance Registry System: methyl 4-[(2-methylbenzoyl)amino]benzoate(200278-95-1)

Safety Data

• Hazardous Substances Data: 200278-95-1(Hazardous Substances Data)

Upstream product

• 933-88-0 ortho-toluoyl chloride 
• 619-45-4 4-methoxycarbonyl aniline 

Downstream Products

• 114341-21-8 2-(p-methoxycarbonylphenyl)phthalimidine 
• 1283597-05-6 2-methyl-N-(4-(5,6,7,12-tetrahydrodibenzo[b,g][1,5]diazocine-6-carbonyl)phenyl)benzamide 
• 169878-67-5 N-[4-[(6,11-Dihydro-5H-dibenz[b,e]azepin-5-yl)-carbonyl]phenyl]-2-methylbenzamide 
• 168078-48-6 2-methyl-N-[4-(pyrrolo[1,2-a]quinoxalin-5(4H)-ylcarbonyl)-phenyl]benzamide 
• 168080-31-7 4-(2-methylbenzoylamino)benzoic acid chloride 
• 108166-22-9 4-[(2-Methylbenzoyl)amino]benzoic acid 

Relevant articles and documents

Copper-Catalyzed sp3 C-H Aminative Cyclization of 2-Alkyl-N-arylbenzamides: An Approach for the Synthesis of N-Aryl-isoindolinones

The synthesis of isoindolinones via copper-catalyzed sp3 C-H functionalization of 2-alkyl-N-substituted benzamides is described. This process does not require the preparation of halogenated substitutes, expensive transition metals, or toxic Sn or CO gas. This method provides an efficient approach to generate various functionalized isoindolinones.

Structure-activity study of novel tricyclic benzazepine arginine vasopressin antagonists

Novel tricyclic benzazepine derivatives were synthesized as arginine vasopressin (AVP) antagonists. Several tricyclic compounds showed potent antagonistic activity in rat AVP receptors V1a and V2. Derivatives containing pyrrolo-tricy