20108-67-2

Basic information

• Product Name: hexaacetyl (-)-chiro-inositol
• CAS NO: 20108-67-2
• Molecular Weight: 432.381
• Mol File: 20108-67-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: hexaacetyl (-)-chiro-inositol(CAS DataBase Reference)
• NIST Chemistry Reference: hexaacetyl (-)-chiro-inositol(20108-67-2)
• EPA Substance Registry System: hexaacetyl (-)-chiro-inositol(20108-67-2)

Safety Data

• Hazardous Substances Data: 20108-67-2(Hazardous Substances Data)

Upstream product

• 108-24-7 acetic anhydride 
• 76235-11-5 deseryladenomycin 
• 64288-00-2 trans-cyclohexa-3,5-diene-1,2-diyl diacetate 
• 17793-95-2 (1RS,2RS)-cyclohexa-3,5-diene-1,2-diol 
• 18685-70-6 chiro-inositol 
• 551-72-4 inositol 
• 488-59-5 myo-inositol 
• 64-17-5 ethanol 
• 4381-96-8 (+/-)-tetra-O-acetylconduritol F 
• 7487-88-9 magnesium sulfate 

Relevant articles and documents

Efficient acylation and one-pot synthesis of dehydroandrographolide succinate on a large scale assisted with microwave radiation

A rapid and convenient method for acylation and large-scale synthesis of dehydroandrographolide succinate has been developed under microwave irradiation. It is a one-pot condensation and is compatible with dehydration and rearrangement of double bond in mild reaction conditions with good yield, high purity (up to 99.8%), time-savings, few pollutants and low cost. In addition, a number of acylation derivatives were synthesized under microwave irradiation.

The structure of adenomycin (C19-97 substance)

-