13719-49-8

Basic information

• Product Name: (E)-N-BENZYL-2-PHENYL-1-ETHENESULFONAMIDE
• Synonyms: (E)-N-benzyl-2-phenylethene-1-sulfonamide;(E)-N-BENZYL-2-PHENYL-1-ETHENESULFONAMIDE
• CAS NO: 13719-49-8
• Molecular Formula: C₁₅H₁₅NO₂S
• Molecular Weight: 273.35
• Mol File: 13719-49-8.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (E)-N-BENZYL-2-PHENYL-1-ETHENESULFONAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-N-BENZYL-2-PHENYL-1-ETHENESULFONAMIDE(13719-49-8)
• EPA Substance Registry System: (E)-N-BENZYL-2-PHENYL-1-ETHENESULFONAMIDE(13719-49-8)

Safety Data

• Hazardous Substances Data: 13719-49-8(Hazardous Substances Data)

Upstream product

• 100-42-5 styrene 
• 52147-97-4 trans 2-phenylethenesulfonyl chloride 
• 100-46-9 benzylamine 

Downstream Products

• 240115-51-9 2-benzyl-2,3-dihydro-1,2-thiazole 1,1-dioxide 

Relevant articles and documents

Diastereoselective synthesis of novel tetra-and pentacyclic annulated coumarino-δ-sultam pyrrolidine, pyrrolizidine, pyrrolothiazole and isoxazolidine derivatives: Via intramolecular 1,3-dipolar cycloadditions

A facile and efficient strategy towards the novel tetra- and pentacyclic annulated coumarino-δ-sultam pyrrolidine, pyrrolizidine, pyrrolothiazole and isoxazolidine via intramolecular 1,3-dipolar cycloadditions of nitrones or azomethine ylides is described

Cyclic sulfonamides via the ring-closing metathesis reaction

The first examples of ring-closing metathesis (RCM) reactions on allyl- and vinylsulfonamide templates 1 and 2 catalyzed by the Grubbs ruthenium alkylidene 3 are described. The rate of cyclization of these reactions are sensitive to simple olefin substitu