129432-24-2

Basic information

• Product Name: 7-O-tert-butyldiphenylsilyl-2,3:5,6-di-O-isopropylidene-1,4-di-O-methylsulphonyl-D-glycero-D-gulo-heptitol
• CAS NO: 129432-24-2
• Molecular Weight: 686.917
• Mol File: 129432-24-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 7-O-tert-butyldiphenylsilyl-2,3:5,6-di-O-isopropylidene-1,4-di-O-methylsulphonyl-D-glycero-D-gulo-heptitol(CAS DataBase Reference)
• NIST Chemistry Reference: 7-O-tert-butyldiphenylsilyl-2,3:5,6-di-O-isopropylidene-1,4-di-O-methylsulphonyl-D-glycero-D-gulo-heptitol(129432-24-2)
• EPA Substance Registry System: 7-O-tert-butyldiphenylsilyl-2,3:5,6-di-O-isopropylidene-1,4-di-O-methylsulphonyl-D-glycero-D-gulo-heptitol(129432-24-2)

Safety Data

• Hazardous Substances Data: 129432-24-2(Hazardous Substances Data)

Upstream product

• 58479-61-1 tert-butylchlorodiphenylsilane 
• 89-67-8 α-D-glucoheptonic γ-lactone 
• 129415-30-1 7-O-tert-butyldiphenylsilyl-2,3:5,6-di-O-isopropylidene-D-glycero-D-gulo-heptono-1,4-lactone 
• 129415-28-7 7-O-tert-butyldiphenylsilyl-D-glycero-D-gulo-heptono-1,4-lactone 
• 129415-35-6 7-O-tert-butyldiphenylsilyl-2,3:5,6-di-O-isopropylidene-D-glycero-D-gulo-heptitol 
• 124-63-0 methanesulfonyl chloride 

Downstream Products

• 129415-37-8 N-benzyl-7-O-tert-butyldiphenylsilyl-1,4-dideoxy-2,3:5,6-di-O-isopropylidene-1,4-imino-D-glycero-D-allo-heptitol 
• 129415-38-9 N-benzyl-1,4-dideoxy-2,3:5,6-di-O-isopropylidene-1,4-imino-D-glycero-D-allo-heptitol 
• 129415-40-3 Methanesulfonate(3aS,3bR,3cR,6aS,8aR)-7a-benzyl-2,2,5,5-tetramethyl-hexahydro-1,3,4,6-tetraoxa-7a-azonia-dicyclopenta[a,f]pentalene; 

Relevant articles and documents

Effect on human liver glycosidases and short syntheses of 1 alpha,2 alpha,6 alpha,7 alpha,7a beta-1,2,6,7-tetrahydroxypyrrolizidine from D-glycero-D-gulo-heptono-1,4-lactone.

The synthesis of 1 alpha,2 alpha,6 alpha,7 alpha,7a beta-1,2,6,7-tetrahydroxypyrrolizidine (1) from D-glycero-D-gulo-heptono-1,4-lactone (6) by two different routes is reported. The effects of 1 on the inhibition of 15 human liver glycosidases are describ