638203-39-1

Basic information

• Product Name: (1R,2R,3R,4S,5S,6R)-2-Allyloxy-3,4,5,6-tetrakis-benzyloxy-cyclohexanol
• Synonyms: (1R,2R,3R,4S,5S,6R)-2-Allyloxy-3,4,5,6-tetrakis-benzyloxy-cyclohexanol
• CAS NO: 638203-39-1
• Molecular Weight: 580.721
• Mol File: 638203-39-1.mol

Chemical Properties

• CAS DataBase Reference: (1R,2R,3R,4S,5S,6R)-2-Allyloxy-3,4,5,6-tetrakis-benzyloxy-cyclohexanol(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2R,3R,4S,5S,6R)-2-Allyloxy-3,4,5,6-tetrakis-benzyloxy-cyclohexanol(638203-39-1)
• EPA Substance Registry System: (1R,2R,3R,4S,5S,6R)-2-Allyloxy-3,4,5,6-tetrakis-benzyloxy-cyclohexanol(638203-39-1)

Safety Data

• Hazardous Substances Data: 638203-39-1(Hazardous Substances Data)

Upstream product

• 637329-52-3 Acetic acid (1S,2S,3R,4R,5S,6R)-2,3,4,5-tetrakis-benzyloxy-6-trifluoromethanesulfonyloxy-cyclohexyl ester 
• 638203-33-5 3,4,5,6-tetra-O-benzyl-1-O-trifluoromethanesulfonyl-L-myo-inositol 
• 637329-53-4 Acetic acid (1R,2S,3R,4S,5R,6S)-2,3,4,5-tetrakis-benzyloxy-6-hydroxy-cyclohexyl ester 
• 638203-45-9 C₄₄H₅₀O₆ 
• 331679-26-6 2,3-O-(D-1,7,7-trimethylbicyclo[2.2.1]hept-6-ylidene)-D-myo-inositol 
• 28140-40-1 1,4,5,6-tetra-O-benzyl-myo-inositol 
• 87-89-8 D-myo-inositol 
• 637329-56-7 Acetic acid (1R,2S,3R,4S,5R,6S)-2-allyloxy-3,4,5,6-tetrakis-benzyloxy-cyclohexyl ester 

Downstream Products

• 637329-58-9 (1S,2R,3S,4R,5S,6R)-2-((2S,3R,4R,5S,6R)-3-Azido-4,5-bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-3,4,5,6-tetrakis-benzyloxy-cyclohexanol 
• 637329-55-6 2-azido-3,4,6-tri-O-benzyl-2-deoxy-D-glucopyranosyl-β-(1->1)-6-O-allyl-2,3,4,5-tetra-O-benzyl-L-chiro-inositol 
• 637329-54-5 2-azido-3,4,6-tri-O-benzyl-2-deoxy-D-glucopyranosyl-α-(1->1)-6-O-allyl-2,3,4,5-tetra-O-benzyl-L-chiro-inositol 

Relevant articles and documents

L-chiro-inositol derivatives from myo-inositol. Building blocks for inositolphosphoglycans

A straightforward synthesis of L-chiro-inositol, deoxy L-chiro-inositol derivatives and L-chiro-inositol building blocks for the preparation of inositolphosphoglycans, is reported from myoinositol. Glycosylation with 2-azido-3,4,6-tri-O-benzyl-2-deoxy-D-g