1242592-27-3

Basic information

• Product Name: N-(4-chlorophenyl)-2-(1-methylethen-1-yl)benzamide
• Synonyms: N-(4-chlorophenyl)-2-(1-methylethen-1-yl)benzamide
• CAS NO: 1242592-27-3
• Molecular Weight: 271.746
• Mol File: 1242592-27-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-(4-chlorophenyl)-2-(1-methylethen-1-yl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-chlorophenyl)-2-(1-methylethen-1-yl)benzamide(1242592-27-3)
• EPA Substance Registry System: N-(4-chlorophenyl)-2-(1-methylethen-1-yl)benzamide(1242592-27-3)

Safety Data

• Hazardous Substances Data: 1242592-27-3(Hazardous Substances Data)

Upstream product

• 577-56-0 2-acetyl-benzoic acid 
• 3609-46-9 2-(prop-1-en-2-yl)benzoic acid 
• 65680-40-2 C₁₀H₉ClO 
• 106-47-8 4-chloro-aniline 
• 7073-70-3 1-bromo-2-isopropenylbenzene 
• 104-12-1 p-chlorphenylisocyanate 

Relevant articles and documents

Enantioselective Palladium(II)-Catalyzed Intramolecular Aminoarylation of Alkenes by Dual N?H and Aryl C?H Bond Cleavage

An asymmetric palladium-catalyzed intramolecular oxidative aminoarylation of alkenes has been developed with quinoline–oxazoline chiral ligands and Ag2CO3 as the oxidant. Various indolines containing a quaternary stereogenic center were synthesized in high yield with excellent enantioselectivity. Preliminary mechanistic studies suggest that the addition of a catalytic amount of phenylglyoxylic acid significantly accelerates the reaction and slightly enhances the enantioselectivity.