1262765-49-0

Basic information

• Product Name: N-[(2E)-1,3-diphenyl-2-propen-1-yl]methanesulfonamide
• Synonyms: N-[(2E)-1,3-diphenyl-2-propen-1-yl]methanesulfonamide
• CAS NO: 1262765-49-0
• Molecular Weight: 287.382
• Mol File: 1262765-49-0.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: N-[(2E)-1,3-diphenyl-2-propen-1-yl]methanesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[(2E)-1,3-diphenyl-2-propen-1-yl]methanesulfonamide(1262765-49-0)
• EPA Substance Registry System: N-[(2E)-1,3-diphenyl-2-propen-1-yl]methanesulfonamide(1262765-49-0)

Safety Data

• Hazardous Substances Data: 1262765-49-0(Hazardous Substances Data)

Upstream product

• 3144-09-0 methanesulfonamide 
• 3412-44-0 (1E)-1,3-diphenylpropene 
• 62668-02-4 (E)-1,3-diphenyl-2-propen-1-ol 

Relevant articles and documents

Electro-oxidative Intermolecular Allylic C(sp3)-H Aminations

The oxidative intermolecular nitrogenation of C(sp3)-H bonds represents one of the most straightforward strategies to construct nitrogen-containing molecules. However, a sacrificial chemical oxidant is generally required. Herein, we describe el

Functional ion liquid method for catalytic synthesis of amine compounds

The invention discloses a method for synthesizing an amine compound catalyzed by functionalized ionic liquid. According to the method, functionalized ionic liquid is used as a catalyst to catalyze N-alkylation of amine and alcohol to synthesize corresponding compound derivatives. Acid functionalized ionic liquid is used as the catalyst to synthesize a series of compounds of amine. The method has the following advantages: a catalytic system is a metal-free system; the usage amount of the catalyst is small, and the catalyst has high catalytic activity, good stability and low corrosivity; operation is simple, and reaction is mild; post-treatment is easy, and the catalyst can be cyclically used.

Efficient ZnBr2-catalyzed reactions of allylic alcohols with indoles, sulfamides and anilines under high-speed vibration milling conditions

Solvent-free reactions of allylic alcohols with various nucleophiles including indoles, sulfamides and anilines were efficiently achieved in the presence of 20% ZnBr2 under high-speed vibration milling conditions, and the products were obtained in good to excellent yields with the formation of water as the only byproduct.