1613415-73-8

Basic information

• Product Name: (R)-4-hexyl-4-(4-methoxyphenyl)-1,2,3-oxathiazolidine 2,2-dioxide
• Synonyms: (R)-4-hexyl-4-(4-methoxyphenyl)-1,2,3-oxathiazolidine 2,2-dioxide
• CAS NO: 1613415-73-8
• Molecular Weight: 313.418
• Mol File: 1613415-73-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R)-4-hexyl-4-(4-methoxyphenyl)-1,2,3-oxathiazolidine 2,2-dioxide(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-4-hexyl-4-(4-methoxyphenyl)-1,2,3-oxathiazolidine 2,2-dioxide(1613415-73-8)
• EPA Substance Registry System: (R)-4-hexyl-4-(4-methoxyphenyl)-1,2,3-oxathiazolidine 2,2-dioxide(1613415-73-8)

Safety Data

• Hazardous Substances Data: 1613415-73-8(Hazardous Substances Data)

Upstream product

• 7019-19-4 1-hydroxyoctan-2-one 
• 1025506-10-8 4-hexyl-5H-[1,2,3]oxathiazole 2,2-dioxide 
• 171364-79-7 2-(4-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 

Relevant articles and documents

Enantioselective rhodium-catalyzed arylation of cyclic N -sulfamidate alkylketimines: A new access to chiral β-alkyl-β-aryl amino alcohols

The enantioselective rhodium-catalyzed 1,2-addition of arylboronates to cyclic N-sulfamidate alkylketimines was developed. With a rhodium/diene complex as catalyst, high enantioselectivity and broad functional group tolerance were observed. The resulting sulfamidates can easily be converted into chiral β-alkyl-β-aryl amino alcohols.