130633-22-6

Basic information

• Product Name: (3aα,4α,5β,7β,7aα)-hexahydro-2,2-dimethylbenzo-1,3(2H)-dioxol-4,5,7-triol
• Synonyms: (3aα,4α,5β,7β,7aα)-hexahydro-2,2-dimethylbenzo-1,3(2H)-dioxol-4,5,7-triol
• CAS NO: 130633-22-6
• Molecular Weight: 204.223
• Mol File: 130633-22-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3aα,4α,5β,7β,7aα)-hexahydro-2,2-dimethylbenzo-1,3(2H)-dioxol-4,5,7-triol(CAS DataBase Reference)
• NIST Chemistry Reference: (3aα,4α,5β,7β,7aα)-hexahydro-2,2-dimethylbenzo-1,3(2H)-dioxol-4,5,7-triol(130633-22-6)
• EPA Substance Registry System: (3aα,4α,5β,7β,7aα)-hexahydro-2,2-dimethylbenzo-1,3(2H)-dioxol-4,5,7-triol(130633-22-6)

Safety Data

• Hazardous Substances Data: 130633-22-6(Hazardous Substances Data)

Upstream product

• 488-73-3 (+)-proto-quercitol 
• 77-76-9 2,2-dimethoxy-propane 

Downstream Products

• 125291-02-3 (1α,2β,3α,4α,5α)-1,2,3,4,5-cyclohexanepentol 1,2,5-trisphosphate 
• 488-73-3 epi-quercitol 
• 125291-05-6 (3aα,4α,5β,7β,7aα)-hexahydro-2,2-dimethylbenzo-1,3(2H)-dioxol-4,5,7-triol tris(dibenzylphosphate) 

Relevant articles and documents

(+)-proto-Quercitol, a natural versatile chiral building block for the synthesis of the α-glucosidase inhibitors, 5-amino-1,2,3,4-cyclohexanetetrols

An efficient synthesis of diastereomerically pure 5-amino-1,2,3,4-cyclohexanetetrols (6 and 11) and quercitol derivatives from naturally available (+)-proto-quercitol (1) is described. The stereochemistry of 1 is perfectly set up for regioselective protec