1597438-09-9

Basic information

• Product Name: 2,3-di-O-benzyl-5,6-O-isopropylidene-D-galactofuranose
• Synonyms: 2,3-di-O-benzyl-5,6-O-isopropylidene-D-galactofuranose
• CAS NO: 1597438-09-9
• Molecular Weight: 400.472
• Mol File: 1597438-09-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,3-di-O-benzyl-5,6-O-isopropylidene-D-galactofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-di-O-benzyl-5,6-O-isopropylidene-D-galactofuranose(1597438-09-9)
• EPA Substance Registry System: 2,3-di-O-benzyl-5,6-O-isopropylidene-D-galactofuranose(1597438-09-9)

Safety Data

• Hazardous Substances Data: 1597438-09-9(Hazardous Substances Data)

Upstream product

• 1597438-00-0 2,3-di-O-benzyl-5,6-O-isopropylidene-D-galactono-1,4-lactone 
• 2782-07-2 D-galactono-1,4-lactone 
• 10257-28-0 D-Galactose 
• 56710-46-4 5,6-O-isopropylidene-D-galactonic acid γ-lactone 

Relevant articles and documents

Synthesis of a novel UDP-carbasugar as UDP-galactopyranose mutase inhibitor

The multistep synthesis of a novel UDP-C-cyclohexene, designed as a high energy intermediate analogue of the UDP-galactopyranose mutase (UGM) catalyzed isomerization reaction, is reported. The synthesis of the central carbasugar involved the preparation of a galactitol derivative bearing two olefins necessary for the construction of the cyclohexene ring by a ring-closing metathesis as a key step. Further successive phosphonylation, deprotection, and UMP coupling provided the target molecule. The final molecule was assayed against UGM and compared with UDP-C-Galf, the C-glycosidic UGM substrate analogue.