227196-07-8

Basic information

• Product Name: L-2,5-di-O-benzyl-chiro-inositol
• Synonyms: L-2,5-di-O-benzyl-chiro-inositol
• CAS NO: 227196-07-8
• Molecular Weight: 360.407
• Mol File: 227196-07-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: L-2,5-di-O-benzyl-chiro-inositol(CAS DataBase Reference)
• NIST Chemistry Reference: L-2,5-di-O-benzyl-chiro-inositol(227196-07-8)
• EPA Substance Registry System: L-2,5-di-O-benzyl-chiro-inositol(227196-07-8)

Safety Data

• Hazardous Substances Data: 227196-07-8(Hazardous Substances Data)

Upstream product

• 594858-42-1 (1R,2S,3S,4R)-1,4-di-O-benzylconduritol B 
• 100-51-6 benzyl alcohol 
• 170210-89-6 (+)-(1S,2R,3R,4S)-1,4-diacetoxy-2,3-dibromocyclohex-5-ene 
• 594858-43-2 2,3-anhydro-1,4-di-O-benzyl-myo-inositol 
• 38876-99-2 1L-chiro-inositol 
• 100-39-0 benzyl bromide 

Downstream Products

• 38876-99-2 1L-chiro-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.