139561-46-9

Basic information

• Product Name: 5a-carba-1,5-anhydro-L-iditol
• Synonyms: 5a-carba-1,5-anhydro-L-iditol
• CAS NO: 139561-46-9
• Molecular Weight: 162.186
• Mol File: 139561-46-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 5a-carba-1,5-anhydro-L-iditol(CAS DataBase Reference)
• NIST Chemistry Reference: 5a-carba-1,5-anhydro-L-iditol(139561-46-9)
• EPA Substance Registry System: 5a-carba-1,5-anhydro-L-iditol(139561-46-9)

Safety Data

• Hazardous Substances Data: 139561-46-9(Hazardous Substances Data)

Upstream product

• 37248-47-8 validamycin A 
• 160651-63-8 2-Deoxy-4,5-O-isopropylidene-3-O-methyl-7-O-tosyl-D-gluco-heptose trimethylene dithioacetal 
• 160651-61-6 2-Deoxy-4,5:6,7-di-O-isopropylidene-3-O-methyl-D-gluco-heptose trimethylene dithioacetal 
• 160651-60-5 2-Deoxy-4,5:6,7-di-O-isopropylidene-D-gluco-heptose trimethylene dithioacetal 
• 160651-62-7 2-Deoxy-4,5-O-isopropylidene-3-O-methyl-D-gluco-heptose trimethylene dithioacetal 
• 160651-64-9 6,7-Anhydro-2-deoxy-4,5-O-isopropylidene-3-O-methyl-D-gluco-heptose trimethylene dithioacetal 
• 160708-47-4 ((3aR)-7c-Methoxy-2,2-dimethyl-(3ar,7at)-3a,4,7,7a-tetrahydro-6H-spirodioxole-5,2'-<1,3>dithian>-4t-yl)methanol 
• 160651-59-2 2-Deoxy-4,5:6,7-di-O-isopropylidene-3-O-tosyl-D-manno-heptose trimethylene dithioacetal 
• 160651-57-0 Trifluoro-methanesulfonic acid (R)-2-[1,3]dithian-2-yl-1-((4R,5S,4'R)-2,2,2',2'-tetramethyl-[4,4']bi[[1,3]dioxolanyl]-5-yl)-ethyl ester 
• 160651-58-1 2-Deoxy-4,5:6,7-di-O-isopropylidene-3-O-methanesulfonyl-D-manno-heptose trimethylene dithioacetal 
• 148324-14-5 2-Deoxy-4,5:6,7-di-O-isopropylidene-D-manno-heptose trimethylene dithioacetal 
• 160708-48-5 2,3-O-Isopropylidene-4-O-methylvalidatol 
• 56180-94-0 acarbose 

Downstream Products

• 102490-49-3 tetra-O-acetyl-(-)-validatol 

Relevant articles and documents

From sugars to carbocycles. 3. Synthesis of validatol and 4-epi-validatol from mannose and glucose

Validatol (4) and 4-epi-validatol (8) are synthesized from mannose and glucose, respectively. The key step in the synthesis of 4 is the base-induced intramolecular displacement reaction of the epoxy dithiane 14 to yield the six-membered carbocycle 15 excl

UNTERSUCHUNGEN ZUR STRUCTUR DES α-D-GLUCOSIDASEINHIBITORS ACARBOSE

Hydrolysis of the pseudotetrasaccharide acarbose (1), a potent inhibitor of intestinal α-D-glucosidases and effective oral antidiabetic agent, gave D-glucose and a tricyclic compound (1R,2S,3R,4aS,7R,8S,8aS,9aR)-1,2,3,4a,7,8,8a,9a-octahydro-1,2,7,8-tetrah