628312-96-9

Basic information

• Product Name: 1,2-O-isopropylidene-3,4,5,6-tetra-O-benzyl-D-chiro-inositol
• Synonyms: 1,2-O-isopropylidene-3,4,5,6-tetra-O-benzyl-D-chiro-inositol
• CAS NO: 628312-96-9
• Molecular Weight: 580.721
• Mol File: 628312-96-9.mol

Chemical Properties

• CAS DataBase Reference: 1,2-O-isopropylidene-3,4,5,6-tetra-O-benzyl-D-chiro-inositol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-O-isopropylidene-3,4,5,6-tetra-O-benzyl-D-chiro-inositol(628312-96-9)
• EPA Substance Registry System: 1,2-O-isopropylidene-3,4,5,6-tetra-O-benzyl-D-chiro-inositol(628312-96-9)

Safety Data

• Hazardous Substances Data: 628312-96-9(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 149820-68-8 1,2-O-isopropylidene-D-chiro-inositol 

Downstream Products

• 260447-16-3 1-D-6-O-allyl-2,3,4,5-tetra-O-benzyl-myo-inositol 
• 202798-30-9 (3aR,4S,5R,6R,7R,7aS)-4,5,6,7-Tetrakis-benzyloxy-hexahydro-benzo[1,3,2]dioxathiole 2,2-dioxide 
• 202845-39-4 Acetic acid (1S,2R,3R,4S,5R,6R)-2,3,4,5-tetrakis-benzyloxy-6-hydroxy-cyclohexyl ester 
• 142436-07-5 2,3,4,5-O-Tetrabenzyl-D-myo-inositol 
• 132437-54-8 1-O-allyl-2,3,4,5-tetra-O-benzyl-D-myo-inositol 
• 627886-31-1 2-azido-3,4,6-tri-O-benzyl-2-deoxy-D-galactopyranosyl-α(1->2)-3,4,5,6-tetra-O-benzol-D-chiro-inositol 
• 627886-43-5 2-azido-3,4,6-tri-O-benzyl-2-deoxy-D-glucopyranosyl-α-(1->2)-3,4,5,6-tetra-O-benzyl-D-chiro-inositol 
• 627886-33-3 3,4,6-tri-O-acetyl-2-azido-2-deoxy-D-galactopyranosyl-α-(1->2)-3,4,5,6-tetra-O-benzyl-D-chiro-inositol 
• 627886-45-7 2-azido-3,4,6-tri-O-acetyl-2-deoxy-D-glucopyranosyl-α(1->2)-3,4,5,6-tetra-O-benzyl-D-chiro-inositol 
• 627886-39-9 2-azido-2-deoxy-D-galactopyranosyl-α-(1->2)-3,4,5,6-tetra-O-benzyl-D-chiro-inositol 
• 202798-29-6 3,4,5,6-tetra-O-benzyl-D-chiro-inositol 

Relevant articles and documents

Synthesis of new hexosaminyl D- and L-chiro-inositols related to putative insulin mediators

We have developed an efficient synthetic strategy to HexNH 2-α(1→3)-L-chiro-inositol (XII-XIII) and HexNH 2-α(1→2)-D-chiro-inositol (XIV-XV) based on the regio and stereoselective glycosylation of tetrabenzoyl-L-chiro-inositol 2 and

Ready routes to key myo-inositol component of GPIs employing microbial arene oxidation or Ferrier reaction

Microbial arene oxidation or Ferrier reaction of enol acetates provides versatile complementary routes that greatly facilitate preparation of inositol synthon(s) for GPI assembly.