49747-42-4

Basic information

• Product Name: N-(2-phenylethenyl)benzamide
• CAS NO: 49747-42-4
• Molecular Formula: C₁₅H₁₃NO
• Molecular Weight: 223.2698
• Mol File: 49747-42-4.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 433.4°C at 760 mmHg
• Flash Point: 260.7°C
• Density: 1.123g/cm³
• Vapor Pressure: 1.03E-07mmHg at 25°C
• Refractive Index: 1.63
• CAS DataBase Reference: N-(2-phenylethenyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-phenylethenyl)benzamide(49747-42-4)
• EPA Substance Registry System: N-(2-phenylethenyl)benzamide(49747-42-4)

Safety Data

• Hazardous Substances Data: 49747-42-4(Hazardous Substances Data)

Upstream product

• 103-64-0 bromostyrene 
• 55-21-0 benzamide 
• 3278-14-6 N-phenethylbenzamide 
• 6502-38-1 chalcone oxime 
• 4231-62-3 1-benzoyl-1H-benzotriazole 
• 102-96-5 (2-nitroethenyl)benzene 
• 98-88-4 benzoyl chloride 
• 101-41-7 benzeneacetic acid methyl ester 
• 98596-77-1 2-Benzoylamino-1-phenyl-1-methoxycarbonyl-aethylen 
• 91632-46-1 2-Benzoylamino-1-phenyl-1-carboxy-aethylen 
• 109393-37-5 2-Benzamido-1-phenylethyl acetate 

Downstream Products

• 1192739-73-3 4-(methylthio)-2,5-diphenylpyrimidine 
• 1192739-66-4 4-(2,5-diphenylpyrimidin-4-yl)morpholine 
• 28660-35-7 (2-amino-1-phenylethyl)phosphonic acid 
• 1445802-43-6 C₁₅H₁₄FNO₂ 
• 3297-72-1 1-phenylisoquinoline 

Relevant articles and documents

Nickel-Catalyzed Reductive Cross-Coupling of N-Acyl and N-Sulfonyl Benzotriazoles with Diverse Nitro Compounds: Rapid Access to Amides and Sulfonamides

Herein we report a Ni-catalyzed reductive transamidation of conveniently available N-acyl benzotriazoles with alkyl, alkenyl, and aryl nitro compounds, which afforded various amides with good yields and a broad substrate scope. The same catalytic reaction conditions were also applicable for N-sulfonyl benzotriazoles, which could undergo smooth reductive coupling with nitroarenes and nitroalkanes to afford the corresponding sulfonamides.

Nickel catalyzed addition of -NH- containing compounds to vinyl and aryl halides

A process for producing unsaturated nitrogen containing compounds such as enamides, enamines and aryl amines/amides is disclosed. A vinyl halide or aryl halide is reacted with an -NH- containing compound in the presence of a catalytic amount of a catalyst precursor composition comprising zero-valent nickel and an organophosphine ligand. One step coupling of vinyl halides and aryl halides with -NH- containing compounds is made possible by practice of this invention.

DEMONSTRATION, CONVERSION AND PROPERTIES OF ENAMIDES. 7. ON RESEARCH ON

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