124601-98-5

Basic information

• Product Name: 4-O-BENZYL-1,2:5,6-DI-O-CYCLOHEXYLIDENE-L-MYO-INOSITOL
• Synonyms: 4-O-BENZYL-1,2:5,6-DI-O-CYCLOHEXYLIDENE-L-MYO-INOSITOL;6-O-BENZYL-2,3:4,5-DI-O-CYCLOHEXYLIDENE-D-MYO-INOSITOL
• CAS NO: 124601-98-5
• Molecular Formula: C₂₅H₃₄O₆
• Molecular Weight: 430.538
• Mol File: 124601-98-5.mol
• Article Data: 16

Chemical Properties

• Boiling Point: 598.5±50.0 °C(Predicted)
• Appearance: /
• Density: 1.27±0.1 g/cm3(Predicted)
• PKA: 13.14±0.40(Predicted)
• CAS DataBase Reference: 4-O-BENZYL-1,2:5,6-DI-O-CYCLOHEXYLIDENE-L-MYO-INOSITOL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-O-BENZYL-1,2:5,6-DI-O-CYCLOHEXYLIDENE-L-MYO-INOSITOL(124601-98-5)
• EPA Substance Registry System: 4-O-BENZYL-1,2:5,6-DI-O-CYCLOHEXYLIDENE-L-MYO-INOSITOL(124601-98-5)

Safety Data

• Hazardous Substances Data: 124601-98-5(Hazardous Substances Data)

Upstream product

• 932-92-3 cyclohexyl ethyl ether 
• 100-39-0 benzyl bromide 
• 6763-49-1 (±)-1,2:3,4-di-O-cyclohexylidene-myo-inositol 
• 6763-49-1 (+/-)-1,2:5,6-dicyclohexylidene-myo-inositol 
• 87-89-8 D-myo-inositol 
• 41545-19-1 (+)-1,2:5,6-di-O-cyclohexylidene-myo-inositol 
• 1122-84-5 1-ethoxycyclohexene 
• 34395-04-5 1,2:3,4-di-O-cyclohexylidene-cis-inositol 
• 40773-58-8 DL-6-O-Benzyl-1,2:3,4-di-O-cyclohexylidene-myo-inositol 
• 129670-42-4 DL-6-O-Benzyl-1,2:3,4-di-O-cyclohexylidene-5-O-tosyl-myo-inositol 
• 131373-23-4 DL-6-O-Benzyl-1,2:3,4-di-O-cyclohexylidene-5-O-propionyl-neo-inositol 
• 933-40-4 cycloxexanone dimethyl ketal 
• 889659-13-6 1-O-butyryl-2,3:4,5-di-O-cyclohexylidene-myo-inositol 
• 124575-20-8 C₄₀H₆₄O₁₀ 

Downstream Products

• 180794-80-3 (-)-6-O-benzyl-2,3:4,5-di-O-cyclohexylidene-1-O-(p-methoxybenzyl)-myo-inositol 
• 418785-06-5 6-O-benzyl-O-(3,4,6-tri-O-acetyl-2-deoxy-2-azido-α-D-glucopyranosyl)-(1→1)-2,3:4,5-di-O-cyclohexylidene-D-myo-inositol 
• 142544-26-1 DL-1,2,3,4-Tetra-O-acetyl-5-deoxy-5-fluoro-myo-inositol 
• 129670-43-5 DL-1,2,3,4-Tetra-O-acetyl-6-O-benzyl-5-deoxy-5-fluoro-myo-inositol 
• 114716-83-5 5-deoxy-5-fluoro-myo-inositol 
• 114656-56-3 C₂₅H₃₃FO₅ 
• 131373-23-4 DL-6-O-Benzyl-1,2:3,4-di-O-cyclohexylidene-5-O-propionyl-neo-inositol 
• 40773-58-8 DL-6-O-Benzyl-1,2:3,4-di-O-cyclohexylidene-neo-inositol 
• 889659-14-7 6-O-benzyl-2,3:4,5-di-O-cyclohexylidene-5-O-(o-xylylenedioxyphosphoryl)-D-myo-inositol 
• 889659-15-8 6-O-benzyl-2,3-β-cyclohexylidene-5-O-(o-xylylenedioxyphosphoryl)-D-myo-inositol 
• 889659-16-9 6-O-benzyl-4,5-carbonate-2,3-O-cyclohexylidene-5-O-(o-xylylenedioxyphosphoryl)-D-myo-inositol 
• 75802-23-2 1L-1-O-(2-amino-2-deoxy-α-D-glucopyranosyl)-myo-inositol 
• 129189-86-2 C₃₆H₄₇N₃O₁₇ 
• 129189-86-2 C₃₆H₄₇N₃O₁₇ 

Relevant articles and documents

Synthesis of substrate analogues as potential inhibitors for Mycobacterium tuberculosis enzyme MshC

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Total synthesis and proof of structure of mycothiol bimane

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Synthesis of the D-3 series of phosphatidylinositol phosphates

The 3-mono-, 3,4-bis-, and 3,4,5-trisphosphates of L-α-phosphatidyl-D-myo-inositol have been synthesized in their optically active forms from the two enantiomers of 1,2:5,6-di-O-cyclohexylidene-myo-inositol. These chiral precursors were prepared by a facile biocatalytic resolution, in which the 4-butyryl ester of the racemic compound was subjected to enantioselective hydrolysis by porcine pancreatic lipase in a biphasic system. The overall yield from individual chiral precursors ranged from 32% for the 3,4,5-trisphosphate to 39% for the monophosphate.