23393-20-6

Basic information

• Product Name: 1D-3-O-benzyl-1,2:4,5-di-O-cyclohexylidene-myo-inositol
• CAS NO: 23393-20-6
• Molecular Weight: 430.541
• Mol File: 23393-20-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1D-3-O-benzyl-1,2:4,5-di-O-cyclohexylidene-myo-inositol(CAS DataBase Reference)
• NIST Chemistry Reference: 1D-3-O-benzyl-1,2:4,5-di-O-cyclohexylidene-myo-inositol(23393-20-6)
• EPA Substance Registry System: 1D-3-O-benzyl-1,2:4,5-di-O-cyclohexylidene-myo-inositol(23393-20-6)

Safety Data

• Hazardous Substances Data: 23393-20-6(Hazardous Substances Data)

Upstream product

• 34361-60-9 1,2:4,5-dicyclohexylidene-myo-inositol 
• 100-39-0 benzyl bromide 
• 87-89-8 D-myo-inositol 
• 23393-20-6 (+/-)-3-O-benzyl-1,2:4,5-di-O,O-cyclohexylidene-myo-inositol 
• 932-92-3 cyclohexyl ethyl ether 
• 111828-85-4 6-O-Camphanoyl-1,2;4,5-di-O-cyclohexylidene-3-O-benzyl-L-myo-inositol 
• 1122-84-5 1-ethoxycyclohexene 
• 111901-83-8 6-O-Camphanoyl-1,2;4,5-di-O-cyclohexylidene-3-O-benzyl-D-myo-inositol 
• 1670-47-9 1,1-diethoxycyclohexane 
• 108-94-1 cyclohexanone 

Downstream Products

• 170555-90-5 1D-3-O-benzyl-1,2:4,5-di-O-cyclohexylidene-6-O-(4-methoxybenzyl)-myo-inositol 
• 16749-95-4 (+/-) 4-O-benzyl-myo-inositol 
• 68738-29-4 1D-1-O-benzyl-myo-inositol 
• 23393-20-6 D-1-O-benzyl-2,3:5,6-di-O-cyclohexylidene-myo-inositol 
• 68738-30-7 1L-1-O-benzyl-myo-inositol 
• 23393-20-6 1D-3-O-benzyl-1,2:4,5-di-O-cyclohexylidene-myo-inositol 

Relevant articles and documents

First Total Synthesis of Mycothiol and Mycothiol Disulfide

(Matrix presented) The first total synthesis of mycothiol and mycothiol disulfide was achieved by linking D-2,3,4,5,6-penta-O-acetyl-myo-inositol, O-(3,4,6-tri-O-acetyl)-2-azido-2-deoxy-α,β-D-glucopyranosyl) trichloroacetimidate, and N,S-diacetyl-L-cysteine and deprotecting peracetylated mycothiol. The first full spectral characterization is reported for underivatized mycothiol. The structure of mycothiol was confirmed by spectral analysis of the known bimane derivative.

Synthesis of racemic 3-methylphosphonate analogues of myo-inositol 3,4-bis- and 1,3,4-trisphosphate

The partially benzyl protected myo-inositol derivatives 11a and 11b, the C-4 and C-1,4 hydroxyl function(s) of which are protected with temporary trans-prop-1-enyl protecting group(s), were readily converted into the respective title compounds 18a and 18b by sequential methylphosphonylation, mild cleavage of the trans-prop-1-enyl group(s), phosphorylation and removal of all permanent benzyl protecting groups.

Phospholipids chiral at phosphorus. 18. Stereochemistry of phosphatidylinositide-specific phospholipase C1

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