1025506-09-5

Basic information

• Product Name: 4-tert-butyl-5H-[1,2,3]oxathiazole 2,2-dioxide
• Synonyms: 4-tert-butyl-5H-[1,2,3]oxathiazole 2,2-dioxide
• CAS NO: 1025506-09-5
• Molecular Weight: 177.224
• Mol File: 1025506-09-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-tert-butyl-5H-[1,2,3]oxathiazole 2,2-dioxide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-tert-butyl-5H-[1,2,3]oxathiazole 2,2-dioxide(1025506-09-5)
• EPA Substance Registry System: 4-tert-butyl-5H-[1,2,3]oxathiazole 2,2-dioxide(1025506-09-5)

Safety Data

• Hazardous Substances Data: 1025506-09-5(Hazardous Substances Data)

Upstream product

• 38895-88-4 1-hydroxy-3,3-dimethylbutan-2-one 

Relevant articles and documents

Enantioselective synthesis of cyclic sulfamidates by using chiral rhodium-catalyzed asymmetric transfer hydrogenation

Asymmetric transfer hydrogenation (ATH) of cyclic sulfamidate imines 4 and 9, using a HCO2H/Et3N mixture as the hydrogen source and well-defined chiral Rh catalysts (S,S)- or (R,R)-2, CpRhCl(TsDPEN), effectively produces the corresponding cyclic sulfamidates with excellent yields and enantioselectivities at room temperature within 0.5 h. ATH of 4,5-disubstituted imines 9, having preexisting stereogenic centers, is shown to take place with dynamic kinetic resolution.