202798-29-6

Basic information

• Product Name: 3,4,5,6-tetra-O-benzyl-D-chiro-inositol
• Synonyms: 3,4,5,6-tetra-O-benzyl-D-chiro-inositol
• CAS NO: 202798-29-6
• Molecular Weight: 540.656
• Mol File: 202798-29-6.mol

Chemical Properties

• CAS DataBase Reference: 3,4,5,6-tetra-O-benzyl-D-chiro-inositol(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4,5,6-tetra-O-benzyl-D-chiro-inositol(202798-29-6)
• EPA Substance Registry System: 3,4,5,6-tetra-O-benzyl-D-chiro-inositol(202798-29-6)

Safety Data

• Hazardous Substances Data: 202798-29-6(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 898808-35-0 C₄₆H₆₆O₆Si₂ 
• 898808-32-7 2,3,4-tri-O-benzyl-1,6-bis-O-(tert-butyldimethylsilyl)hexane-1,2,3,4,5,6-hexaol 
• 898808-36-1 (2S,3S,4S,5R)-2,3,4,5-Tetrakis-benzyloxy-hexane-1,6-diol 
• 628312-96-9 1,2-O-isopropylidene-3,4,5,6-tetra-O-benzyl-D-chiro-inositol 
• 149820-68-8 1,2-O-isopropylidene-D-chiro-inositol 

Downstream Products

• 215869-20-8 (1S,2S,3S,4R,5R,6S)-2,3,4,5-Tetrakis-benzyloxy-6-(4-methoxy-benzyloxy)-cyclohexanol 
• 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 
• 627886-31-1 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 
• 158340-85-3 1,2,3,4,5-Penta-O-benzyl-D-chiro-inositol 
• 1152292-15-3 2,3,4,6-tetra-O-benzyl-D-mannopyranosyl-α(1->1)-3,4,5,6-tetra-O-benzyl-D-chiro-inositol 
• 1152292-14-2 2,3,4,6-tetra-O-benzyl-D-mannopyranosyl-β(1->2)-3,4,5,6-tetra-O-benzyl-D-chiro-inositol 
• 1152292-13-1 2,3,4,6-tetra-O-benzyl-D-mannopyranosyl-α(1->2)-3,4,5,6-tetra-O-benzyl-D-chiro-inositol 
• 1152618-97-7 2,3,4,6-tetra-O-acetyl-D-mannopyranosyl-α(1->2)-3,4,5,6-tetra-O-benzyl-D-chiro-inositol 
• 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 
• 899438-04-1 1-O-(3,4,6-tri-O-benzyl-2-benzyloxycarboxamido-2-deoxy-β-D-galactopyranosyl)-2,3,4,5,6-penta-O-benzyl-D-chiro-inositol 

Relevant articles and documents

Synthesis of galactosaminyl d-chiro-inositols

All six isomeric d-galactosaminopyranosyl-d-chiro-inositols have been prepared by glycosylation of appropriate penta-O-benzyl-d-chiro-inositols. The three requisite protected d-chiro-inositols were prepared by SmI2-promoted pinacol coupling of

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.

Synthesis of a jojoba bean disaccharide

A synthesis of the disaccharide recently isolated from jojoba beans, 2-O-α-D-galactopyranosyl-D-chiro-inositol, has been achieved. The suitably protected chiro-inositol unit was prepared by an enantiospecific synthesis from L-xylose utilizing SmI2-mediated pinacol coupling as a key step. Copyright (C) 1998 Elsevier Science Ltd.