231618-84-1

Basic information

• Product Name: (4R,5R,6R)-1-<(tert-butyldimethylsilyl)oxy>-6-<((chloromethyl)sulfonyl)oxy>-4,5,7-tris(benzyloxy)-2(E)-heptene
• Synonyms: (4R,5R,6R)-1-<(tert-butyldimethylsilyl)oxy>-6-<((chloromethyl)sulfonyl)oxy>-4,5,7-tris(benzyloxy)-2(E)-heptene
• CAS NO: 231618-84-1
• Molecular Weight: 675.358
• Mol File: 231618-84-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (4R,5R,6R)-1-<(tert-butyldimethylsilyl)oxy>-6-<((chloromethyl)sulfonyl)oxy>-4,5,7-tris(benzyloxy)-2(E)-heptene(CAS DataBase Reference)
• NIST Chemistry Reference: (4R,5R,6R)-1-<(tert-butyldimethylsilyl)oxy>-6-<((chloromethyl)sulfonyl)oxy>-4,5,7-tris(benzyloxy)-2(E)-heptene(231618-84-1)
• EPA Substance Registry System: (4R,5R,6R)-1-<(tert-butyldimethylsilyl)oxy>-6-<((chloromethyl)sulfonyl)oxy>-4,5,7-tris(benzyloxy)-2(E)-heptene(231618-84-1)

Safety Data

• Hazardous Substances Data: 231618-84-1(Hazardous Substances Data)

Upstream product

• 18162-48-6 tert-butyldimethylsilyl chloride 
• 160549-10-0 2,3,5-tri-O-benzyl-D-arabinofuranose 
• 3518-65-8 monochloromethanesulfonyl chloride 
• 172986-75-3 (4R,5R,6R)-1-<(tert-butyldimethylsilyl)oxy>-4,5,7-tris(benzyloxy)-2(E)-hepten-6-ol 
• 231618-83-0 (4R,5R,6R)-4,5,7-tris(benzyloxy)-2(E)-heptene-1,6-diol 
• 146346-44-3 methyl (4R,5R,6R)-6-hydroxy-4,5,7-tris(benzyloxy)-2(E)-heptenoate 

Downstream Products

• 172986-77-5 (4R,5R,6S)-6-<((chloromethyl)sulfonyl)oxy>-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 
• 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 
• 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 
• 231618-85-2 (4R,5R,6S)-1-<(tert-butyldimethylsilyl)oxy>-6-<((chloromethyl)sulfonyl)oxy>-4,5,7-tris(benzyloxy)-2(E)-heptene 
• 172986-76-4 (4R,5R,6S)-6-acetoxy-1-<(tert-butyldimethylsilyl)oxy>-4,5,7-tris(benzyloxy)-2(E)-heptene 

Relevant articles and documents

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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