149820-68-8

Basic information

• Product Name: 1,2-O-isopropylidene-D-chiro-inositol
• Synonyms: 1,2-O-isopropylidene-D-chiro-inositol
• CAS NO: 149820-68-8
• Molecular Weight: 220.222
• Mol File: 149820-68-8.mol

Chemical Properties

• CAS DataBase Reference: 1,2-O-isopropylidene-D-chiro-inositol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-O-isopropylidene-D-chiro-inositol(149820-68-8)
• EPA Substance Registry System: 1,2-O-isopropylidene-D-chiro-inositol(149820-68-8)

Safety Data

• Hazardous Substances Data: 149820-68-8(Hazardous Substances Data)

Upstream product

• 77-76-9 2,2-dimethoxy-propane 

Downstream Products

• 488-54-0 D-chiro-inositol 
• 488-54-0 neo-inositol 
• 628312-96-9 1,2-O-isopropylidene-3,4,5,6-tetra-O-benzyl-D-chiro-inositol 
• 1152292-08-4 1,2-O-isopropyliden-3,4,5,6-tetra-O-benzoyl-D-chiro-inositol 
• 111446-91-4 (+/-)-3,4,6-tri-O-benzyl-1,2-O-isopropylidene-myo-inositol 
• 131146-89-9 (+/-)-1,5,6-tri-O-benzyl-2,3-O-isopropylidene-myo-inositol 
• 98906-25-3 (±)-1,2-O-isopropylidene-3,6-di-O-benzyl-myo-inositol 
• 29847-13-0 (±)-1,4,5,6-tetra-O-benzyl-2,3-O-isopropylidene-myo-inositol 
• 99756-37-3 (±)-3,6-di-O-benzoyl-1,2:4,5-di-O-isopropylidene-myo-inositol 
• 115072-66-7 (±)-3,4-di-O-benzoyl-1,2:5,6-di-O-isopropylidene-myo-inositol 
• 115072-69-0 5,6-di-O-allyl-1,2:3,4-di-O-isopropylidene-myo-inositol 
• 51548-88-0 (+/-)-1,2:4,5-di-O-isopropylidene-myo-inositol 
• 26276-99-3 rac-1,4,5,6-tetra-O-benzyl-myo-inositol 
• 38643-30-0 (±)-1,2:5,6-di-O-isopropylidene-myo-inositol 

Relevant articles and documents

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

Synthesis of all possible regioisomers of myo-inositol pentakisphosphate

Synthesis of all possible 4 regioisomers of IP5, naturally occurring metabolites of IP3 and IP4, was accomplished from myo-inositol via its monobenzoate derivatives (IBz1) as the key intermediates; base-catalyzed isomerization of readily available IBz1 derivatives, followed by suitable separation procedures efficiently provided the requisite regioisomers of IBz1.