942066-43-5

Basic information

• Product Name: tert-butyl N-[(3-hydroxy-4-(benzyloxy)butyl)sulfonyl]carbamate
• Synonyms: tert-butyl N-[(3-hydroxy-4-(benzyloxy)butyl)sulfonyl]carbamate
• CAS NO: 942066-43-5
• Molecular Weight: 359.444
• Mol File: 942066-43-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: tert-butyl N-[(3-hydroxy-4-(benzyloxy)butyl)sulfonyl]carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl N-[(3-hydroxy-4-(benzyloxy)butyl)sulfonyl]carbamate(942066-43-5)
• EPA Substance Registry System: tert-butyl N-[(3-hydroxy-4-(benzyloxy)butyl)sulfonyl]carbamate(942066-43-5)

Safety Data

• Hazardous Substances Data: 942066-43-5(Hazardous Substances Data)

Upstream product

• 2930-05-4 Benzyloxymethyl-oxiran 
• 147751-16-4 tert-butyl (methylsulfonyl)carbamate 

Downstream Products

• 67838-55-5 (±)-3-benzyloxymethyl-1,2-thiazolidine 1,1-dioxide 
• 942066-34-4 3-(benzyloxymethyl)-4,5-dihydro-isothiazole 1,1-dioxide 

Relevant articles and documents

Synthesis of chiral γ-sultams through intramolecular reductive amination with sulfonylcarbamate as N-source

An efficient and enantioselective palladium-catalyzed intramolecular asymmetric reductive amination with sulfonylcarbamates as N-sources was reported, providing a facile and general access to the chiral γ-sultam derivatives with up to 97% of enantioselect