778561-25-4

Basic information

• Product Name: 3,4-Pyrrolidinediol,2-[(1R)-1-hydroxyethyl]-,(2S,3S,4R)-(9CI)
• Synonyms: 3,4-Pyrrolidinediol,2-[(1R)-1-hydroxyethyl]-,(2S,3S,4R)-(9CI)
• CAS NO: 778561-25-4
• Molecular Formula: C6H13NO3
• Molecular Weight: 0
• Product Categories: ALCOHOL
• Mol File: 778561-25-4.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3,4-Pyrrolidinediol,2-[(1R)-1-hydroxyethyl]-,(2S,3S,4R)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-Pyrrolidinediol,2-[(1R)-1-hydroxyethyl]-,(2S,3S,4R)-(9CI)(778561-25-4)
• EPA Substance Registry System: 3,4-Pyrrolidinediol,2-[(1R)-1-hydroxyethyl]-,(2S,3S,4R)-(9CI)(778561-25-4)

Safety Data

• Hazardous Substances Data: 778561-25-4(Hazardous Substances Data)

Upstream product

• 60409-15-6 D-perosamide 
• 92898-55-0 (2R,3S,4S)-2<(1R)-1-Hydroxyethyl>-1-<(1S)-(1,4,6/5)-4,5,6-trihydroxy-3-hydroxymethyl-2-cyclohexenyl>-3,4-pyrrolidindiol 
• 610314-63-1 N-(2,2-di(ethoxycarbonyl)vinyl)-4-O-mesyl-2,3-O-(4-methoxybenzylidene)-β-L-rhamnopyranosylamine 
• 678142-31-9 N-(2,2-di(ethoxycarbonyl)vinyl)-2,3-O-(4-methoxybenzylidene)-β-L-rhamnopyranosylamine 
• 678142-32-0 N-(2,2-di(ethoxycarbonyl)vinyl)-4-O-mesyl-β-L-rhamnopyranosylamine 
• 610314-57-3 1,4-anhydro-2,3-di-O-benzoyl-N-(2,2-di(ethoxycarbonyl)vinyl)-β-L-rhamnopyranosylamine 
• 92621-73-3 (1R,2S,3R,4aS,7R,8S,8aS,9aR)1,2,3,4a,7,8,8a,9a-Octahydro-1,2,7,8-tetrahydroxy-3-<(R)-1-hydroxyethyl>-6-hydroxymethylpyrrolo<2,1-b>benzoxazol 
• 56180-94-0 acarbose 

Relevant articles and documents

Anhydroazasugars as key intermediates in the stereocontrolled preparation of azasugars and their ethyl thioglycosides

Bicyclic azasugar thioglycosides, a new type of azasugar and alkaloid derivative, are stereoselectively prepared from easily available glycosylenamines (D-gluco and L-rhamno configurations), via 1,4-anhydroazasugar derivatives. Polyhydroxylated pyrrolidines (nonreducing pyrrolidine azasugars) are also prepared by reduction with sodium cyanoborohydride of the same 1,4-anhydroazasugars. The stereochemical assignments of the new stereogenic centres are based on NMR experiments, including a study of the interproton distances from quantitative treatment of NOE data and molecular modeling.

DERIVATIVES OF 1,4-DIDEOXY-1,4-IMINO-D-MANNITOL AND A PROCESS FOR THEIR PREPARATTON

Novel derivatives of 1,4-dideoxy-1,4-imino-D-mannitol and method for their synthesis from 4,5-anhydro-1-azido-1-deoxy-2,3-O-isopropylidene-D-talitol or its triflate derivative are disclosed. The novel derivatives, 6-fluoro-1,4-imino-1,4,6-trideoxy-D-manni

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