461383-64-2

Basic information

• Product Name: S-(2-iodophenethyl) 2-(2-azidoethyl)benzenecarbothioate
• CAS NO: 461383-64-2
• Molecular Weight: 437.304
• Mol File: 461383-64-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: S-(2-iodophenethyl) 2-(2-azidoethyl)benzenecarbothioate(CAS DataBase Reference)
• NIST Chemistry Reference: S-(2-iodophenethyl) 2-(2-azidoethyl)benzenecarbothioate(461383-64-2)
• EPA Substance Registry System: S-(2-iodophenethyl) 2-(2-azidoethyl)benzenecarbothioate(461383-64-2)

Safety Data

• Hazardous Substances Data: 461383-64-2(Hazardous Substances Data)

Upstream product

• 25109-86-8 methyl 2-(2-bromoethyl)benzoate 
• 461383-54-0 methyl 2-(2-azidoethyl)benzoate 
• 461383-55-1 2-(2-azidoethyl)benzoic acid 
• 177748-62-8 2-(2-iodophenyl)-1-ethanethiol 
• 461383-56-2 2-(2-azidoethyl)benzoyl chloride 

Downstream Products

• 4565-32-6 2,3-dihydrobenzo(b)thiophene 
• 1196-38-9 3,4-dihydroisoquinolin-1(2H)-one 

Relevant articles and documents

Intramolecular Cyclization of Acyl Radicals onto the Azido Group: A New Radical Approach to Cyclized Lactams

(Equation Presented) Reagents: i, Bu3SnH/AlBN; ii, (TMS)3SiH/AlBN. Aryl- and alkyl-derived azidoacyl radicals, generated from thiolesters by intramolecular homolytic substitution at the sulfur, can undergo five- and six-membered cyclization onto the azido moiety to give cyclized lactams.