79391-04-1

Basic information

• Product Name: D-chiro-Inositol, 2-O-.alpha.-D-galactopyranosyl-
• Synonyms: D-chiro-Inositol, 2-O-.alpha.-D-galactopyranosyl-
• CAS NO: 79391-04-1
• Molecular Formula: C₁₂H₂₂O₁₁
• Molecular Weight: 342.29648
• Mol File: 79391-04-1.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: D-chiro-Inositol, 2-O-.alpha.-D-galactopyranosyl-(CAS DataBase Reference)
• NIST Chemistry Reference: D-chiro-Inositol, 2-O-.alpha.-D-galactopyranosyl-(79391-04-1)
• EPA Substance Registry System: D-chiro-Inositol, 2-O-.alpha.-D-galactopyranosyl-(79391-04-1)

Safety Data

• Hazardous Substances Data: 79391-04-1(Hazardous Substances Data)

Upstream product

• 215869-20-8 (1S,2S,3S,4R,5R,6S)-2,3,4,5-Tetrakis-benzyloxy-6-(4-methoxy-benzyloxy)-cyclohexanol 
• 215869-70-8 1,2,3,4,6-penta-O-benzyl-D-chiro-inositol 
• 202798-29-6 3,4,5,6-tetra-O-benzyl-D-chiro-inositol 
• 74808-09-6 2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl trichloroacetimidate 
• 781616-21-5 2,3,4,6-tetra-O-benzyl-D-galactopyranosyl-α(1->2)-D-chiro-inositol 
• 215869-71-9 (2R,3S,4S,5R,6R)-3,4,5-Tris-benzyloxy-2-benzyloxymethyl-6-((2S,3R,5R,6S)-2,3,4,5,6-pentakis-benzyloxy-cyclohexyloxy)-tetrahydro-pyran 
• 87-89-8 D-myo-inositol 
• 210281-95-1 β-D-mannopyranosyl fluoride 
• 439-03-2 2,3,4,6-tetra-O-acetyl-β-D-mannopyranosyl fluoride 
• 28140-37-6 3,4,6-tri-O-acetyl-1,2-O-(1-ethoxyethylidene)-β-D-mannopyranoside 
• 6587-77-5 1-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2,3,4,5,6-penta-O-acetyl-sn-myo-inositol 
• 29971-56-0 1-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-3,4,5,6-tetra-O-acetyl-sn-myo-inositol 

Downstream Products

• 59-23-4 D-Galactose 
• 488-54-0 D-chiro-inositol 
• 6587-77-5 1-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2,3,4,5,6-penta-O-acetyl-sn-myo-inositol 

Relevant articles and documents

Creation of an α-mannosynthase from a broad glycosidase scaffold

α-Mannosides made easy: Mutation of a family-GH31 α-glucosidase that displays plasticity to alterations at the 2-OH position of donor substrates created an efficient α-mannoside-synthesizing biocatalyst. A simple fluoride donor reagent was used for the synthesis of a range of mono-α-mannosylated conjugates using the α-mannosynthase displaying low (unwanted) oligomerization activity. Copyright

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.

Biosynthesis of mannophospholipids by Mycobacterium phlei.

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