220939-98-0

Basic information

• Product Name: ((1R,5R,6S)-5,6-Bis-benzyloxy-1-benzyloxymethyl-cyclohex-3-enyloxy)-trimethyl-silane
• Synonyms: ((1R,5R,6S)-5,6-Bis-benzyloxy-1-benzyloxymethyl-cyclohex-3-enyloxy)-trimethyl-silane
• CAS NO: 220939-98-0
• Molecular Weight: 502.726
• Mol File: 220939-98-0.mol

Chemical Properties

• CAS DataBase Reference: ((1R,5R,6S)-5,6-Bis-benzyloxy-1-benzyloxymethyl-cyclohex-3-enyloxy)-trimethyl-silane(CAS DataBase Reference)
• NIST Chemistry Reference: ((1R,5R,6S)-5,6-Bis-benzyloxy-1-benzyloxymethyl-cyclohex-3-enyloxy)-trimethyl-silane(220939-98-0)
• EPA Substance Registry System: ((1R,5R,6S)-5,6-Bis-benzyloxy-1-benzyloxymethyl-cyclohex-3-enyloxy)-trimethyl-silane(220939-98-0)

Safety Data

• Hazardous Substances Data: 220939-98-0(Hazardous Substances Data)

Upstream product

• 160549-10-0 2,3,5-tri-O-benzyl-D-arabinofuranose 
• 220939-94-6 (3S,4R)-1,3,4-tris(benzyloxy)-hex-5-en-2-one 

Downstream Products

• 17550-45-7 1α.2β.3α-Trihydroxy-1β-hydroxymethyl-cyclohexan 

Relevant articles and documents

Ring closing metathesis as an efficient approach to branched cyclitols and aminocyclitols: A short synthesis of valiolamine

Ring closing metathesis of sugar-derived 1,6 dienes is the key step for the construction of highly functionnalized cyclohexenes, precursors of branched cyclitols and aminocyclitols. The method has been used for a short synthesis of valiolamine.