475630-67-2

Basic information

• Product Name: 3,4-Piperidinediol,2-(hydroxymethyl)-,(2S,3S,4R)-(9CI)
• Synonyms: 3,4-Piperidinediol,2-(hydroxymethyl)-,(2S,3S,4R)-(9CI)
• CAS NO: 475630-67-2
• Molecular Formula: C6H13NO3
• Molecular Weight: 147.17
• Product Categories: ALCOHOL
• Mol File: 475630-67-2.mol
• Article Data: 35

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3,4-Piperidinediol,2-(hydroxymethyl)-,(2S,3S,4R)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-Piperidinediol,2-(hydroxymethyl)-,(2S,3S,4R)-(9CI)(475630-67-2)
• EPA Substance Registry System: 3,4-Piperidinediol,2-(hydroxymethyl)-,(2S,3S,4R)-(9CI)(475630-67-2)

Safety Data

• Hazardous Substances Data: 475630-67-2(Hazardous Substances Data)

Upstream product

• 98260-69-6 4-O-benzyl-N-benzyloxycarbonyl-1,5-imino-1,2,5-trideoxy-D-arabino-hexitol 
• 104958-79-4 1,2,5-trideoxy-4-O-(β-D-glucopyranosyl)-1,5-imino-D-arabinohexitol 
• 121742-14-1 (3S,4R)-6-[(benzyloxycarbonyl)amino]-5,6-dideoxyhex-2-ulose 
• 143706-32-5 2-Desoxy-L-threo-5-hexulosonitril 
• 65564-05-8 3-[(benzyloxycarbonyl)amino]propanal 
• 354153-41-6 (1S,2R,6R)-2-(tert-butyldiphenylsilanyloxymethyl)-7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylic acid tert-butyl ester 
• 354153-40-5 (1R,2R,6S)-2-(tert-butyldiphenylsilanyloxymethyl)-7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylic acid tert-butyl ester 
• 768387-41-3 (4aR,8R,8aR)-tert-butyl hexahydro-8-hydroxy-2,2-dimethyl[1,3]dioxino[5,4-b]pyridine-5-carboxylate 
• 943135-43-1 3,4-dibenzyloxy-1,5-imino-1,2,5-trideoxy-D-arabino hexitol 
• 943135-45-3 (2R,3R)-5-[N-(tert-butoxycarbonyl)amino]-2,3-dibenzyloxy-1-(tert-butyl-dimethylsilyloxy)pentane 
• 943135-38-4 (2R,3R)-5-[N-(tert-butoxycarbonyl)amino]-2,3-dibenzyloxypentan-1-ol 
• 943135-46-4 (2S,3R)-5-[N-(tert-butoxycarbonyl)amino]-2,3-dibenzyloxypentanal 
• 943135-42-0 ethyl (4R,5R)-7-[N-(tert-butoxycarbonyl)amino]-4,5-dibenzyloxy-2-heptenoate 
• 943135-39-5 (4R,5R)-7-[N-(tert-butoxycarbonyl)amino]-4,5-dibenzyloxy-2-hepten-1-ol 

Relevant articles and documents

LACK OF GLYCOSIDASE INHIBITION BY, AND ISOLATION FROM XANTHOCERCIS ZAMBESIACA (LEGUMINOSAE) OF, 4-O-(&β-D-GLUCOPYRANOSYL)-FAGOMINE , A NOVEL GLUCOSIDE OF POLYHYDROXYLATED PIPERIDINE ALKALOID

A COSY spectrum has been used to determine the position of inter-residue linkage in 4-O-(β-D-glucopyranosyl) fagomine (1) an example of a new class of glycosides of polyhydroxylated piperidine alkaloids isolated from seed of the legume Xanthocercis zambesiaca. (Bak.) Dunn.Unlike a number of polyhydroxylated piperidines, neither the glucoside (1) nor the fagomine (3) showed any inhibitory activity towards glycosidase enzymes from a variety of sources.

N-Containing sugars from Morus alba and their glycosidase inhibitory activities

The reexamination of N-containing sugars from the roots of Morus alba by improved purification procedures led to the isolation of eighteen N-containing sugars, including seven that were isolated from the leaves of Morus bombycis.These N-containing sugars

Organocatalyzed synthesis of (-)-4-epi-fagomine and the corresponding pipecolic acids

The enantioselective synthesis of 4-epi-fagomine was accomplished starting from dioxanone and Cbz-protected benyzlamine, in 4 steps, with 18% overall yield. The key feature of this synthetic approach is the tactical combination of reactions: organocatalyz

A PROCESS FOR SYNTHESIS OF PIPERIDINE ALKALOIDS

The present invention discloses a process for synthesis of piperidine alkaloids selected from fagomine, 4-epi-fagomine and nojirimycin from tri-O-benzyl-D-glucal or tri-O-benzyl-D-galactal.