172986-75-3

Basic information

• Product Name: (4R,5R,6R)-1-<(tert-butyldimethylsilyl)oxy>-4,5,7-tris(benzyloxy)-2(E)-hepten-6-ol
• Synonyms: (4R,5R,6R)-1-<(tert-butyldimethylsilyl)oxy>-4,5,7-tris(benzyloxy)-2(E)-hepten-6-ol
• CAS NO: 172986-75-3
• Molecular Weight: 562.822
• Mol File: 172986-75-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (4R,5R,6R)-1-<(tert-butyldimethylsilyl)oxy>-4,5,7-tris(benzyloxy)-2(E)-hepten-6-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (4R,5R,6R)-1-<(tert-butyldimethylsilyl)oxy>-4,5,7-tris(benzyloxy)-2(E)-hepten-6-ol(172986-75-3)
• EPA Substance Registry System: (4R,5R,6R)-1-<(tert-butyldimethylsilyl)oxy>-4,5,7-tris(benzyloxy)-2(E)-hepten-6-ol(172986-75-3)

Safety Data

• Hazardous Substances Data: 172986-75-3(Hazardous Substances Data)

Upstream product

• 18162-48-6 tert-butyldimethylsilyl chloride 
• 231618-83-0 (4R,5R,6R)-4,5,7-tris(benzyloxy)-2(E)-heptene-1,6-diol 
• 160549-10-0 2,3,5-tri-O-benzyl-D-arabinofuranose 
• 146346-44-3 methyl (4R,5R,6R)-6-hydroxy-4,5,7-tris(benzyloxy)-2(E)-heptenoate 

Downstream Products

• 231618-85-2 (4R,5R,6S)-1-<(tert-butyldimethylsilyl)oxy>-6-<((chloromethyl)sulfonyl)oxy>-4,5,7-tris(benzyloxy)-2(E)-heptene 
• 231619-07-1 (2R,3S,4S,5R,6S)-6-<((chloromethyl)sulfonyl)oxy>-2,3-epoxy-4,5,7-tris(benzyloxy)-2(E)-hepten-1-ol 
• 231619-06-0 (2S,3R,4S,5R,6S)-6-<((chloromethyl)sulfonyl)oxy>-2,3-epoxy-4,5,7-tris(benzyloxy)-2(E)-hepten-1-ol 
• 173142-25-1 (4R,5R,6S)-1-<(tert-butyldimethylsilyl)oxy>-4,5,7-tris(benzyloxy)-2(E)-hepten-6-ol 
• 172986-77-5 (4R,5R,6S)-6-<((chloromethyl)sulfonyl)oxy>-4,5,7-tris(benzyloxy)-2(E)-hepten-1-ol 
• 172986-76-4 (4R,5R,6S)-6-acetoxy-1-<(tert-butyldimethylsilyl)oxy>-4,5,7-tris(benzyloxy)-2(E)-heptene 
• 231618-84-1 (4R,5R,6R)-1-<(tert-butyldimethylsilyl)oxy>-6-<((chloromethyl)sulfonyl)oxy>-4,5,7-tris(benzyloxy)-2(E)-heptene 

Relevant articles and documents

Iminocyclitol inhibitors of hexoaminidase and glycosidase

Designed iminocylitols that have potent inhibition activity with respect to hexominidases and glycosides are disclosed.

Synthesis and inhibition analysis of five-membered homoazasugars from D-arabinofuranose via an SN2 reaction of the chloromethylsulfonate

Five-membered homoazasugars having a side-chain which can be modified to other functional groups or linked to other aglycon moieties were prepared from 2,3,5-tri-O-benzyl-D-arabinofuranose via a favorable SN2 reaction of the chloromethylsulfonate with azi