3096-94-4

Basic information

• Product Name: N-(2,3-dimethylphenyl)benzamide
• Synonyms: N-(2,3-dimethylphenyl)benzamide;BENZAMIDE, N-(2,3-DIMETHYLPHENYL)-;2',3'-BENZOXYLIDIDE
• CAS NO: 3096-94-4
• Molecular Formula: C₁₅H₁₅NO
• Molecular Weight: 225.29
• Mol File: 3096-94-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 282.1°C at 760 mmHg
• Flash Point: 167.4°C
• Appearance: /
• Density: 1.121g/cm³
• Vapor Pressure: 0.00342mmHg at 25°C
• Refractive Index: 1.619
• CAS DataBase Reference: N-(2,3-dimethylphenyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2,3-dimethylphenyl)benzamide(3096-94-4)
• EPA Substance Registry System: N-(2,3-dimethylphenyl)benzamide(3096-94-4)

Safety Data

• Hazardous Substances Data: 3096-94-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C15H15NO/c1-11-7-6-10-14(12(11)2)16-15(17)13-8-4-3-5-9-13/h3-10H,1-2H3,(H,16,17)

Upstream product

• 98-88-4 benzoyl chloride 
• 87-59-2 2,3-Dimethylaniline 
• 357163-95-2 1-(2,3-dimethylphenyl)-1H-1,2,3,4-tetrazole 
• 100-52-7 benzaldehyde 

Downstream Products

• 66354-67-4 4-methyl-2-phenyl-1H-indole 
• 925442-12-2 4-(benzoylamino)-2,3-dimethylbenzaldehyde 
• 1383796-94-8 5-methyl-2-phenyl-4H-benzo[d][1,3]oxazine 

Relevant articles and documents

Cross-Dehydrogenating Coupling of Aldehydes with Amines/R-OTBS Ethers by Visible-Light Photoredox Catalysis: Synthesis of Amides, Esters, and Ureas

A straightforward synthesis of amides, ureas, and esters is reported by visible-light cross-dehydrogenating coupling (CDC) of aldehydes (or amine carbaldehydes) and amines/R-OTBS ethers by photoredox catalysis. The reaction is found to be general and high yielding. A plausible mechanistic pathway has been proposed for these transformations and is supported by appropriate controlled experiments.

Copper-catalyzed selective benzylic C-O cyclization of N-o-tolylbenzamides: Synthesis of 4 H-3,1-benzoxazines

A novel Selectfluor-mediated copper-catalyzed highly selective benzylic C-O cyclization for the synthesis 4H-3,1-benzoxazines is reported. The predominant selectivity for a benzylic C(sp3)-H over an aromatic C(sp 2)-H bond in N-o-tolylbenzamides is achieved.