594858-40-9

Basic information

• Product Name: 1,2,3,4,5,6-Cyclohexanehexol, 1,2,3,4-tetraacetate, (1S,2S,3S,4S,5S,6R)-
• CAS NO: 594858-40-9
• Molecular Formula: C14H20O10
• Molecular Weight: 348.307
• Mol File: 594858-40-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,2,3,4,5,6-Cyclohexanehexol, 1,2,3,4-tetraacetate, (1S,2S,3S,4S,5S,6R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3,4,5,6-Cyclohexanehexol, 1,2,3,4-tetraacetate, (1S,2S,3S,4S,5S,6R)-(594858-40-9)
• EPA Substance Registry System: 1,2,3,4,5,6-Cyclohexanehexol, 1,2,3,4-tetraacetate, (1S,2S,3S,4S,5S,6R)-(594858-40-9)

Safety Data

• Hazardous Substances Data: 594858-40-9(Hazardous Substances Data)

Upstream product

• 170210-89-6 (+)-(1S,2R,3R,4S)-1,4-diacetoxy-2,3-dibromocyclohex-5-ene 
• 182075-57-6 1,2,3,4-tetra-O-acetylconduritol E 

Downstream Products

• 643-10-7 allo-inositol 

Relevant articles and documents

Stereoselective synthesis of myo-, neo-, L-chiro, D-chiro, allo-, scyllo-, and epi-inositol systems via conduritols prepared from p-benzoquinone

A practical route is described for the flexible preparation of a wide variety of inositol stereoisomers and their polyphosphates. The potential of this approach is demonstrated by the synthesis of myo-, L-chiro-, D-chiro-, epi-, scyllo-, allo-, and neo-inositol systems. Optically pure compounds in either enantiomeric form can be prepared from p-benzoquinone via enzymatic resolution of a derived conduritol B key intermediate. High-performance anion-exchange chromatography with pulsed amperometric detection permits inositol stereoisomers to be resolved and detected with high sensitivity. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.