41545-19-1

Basic information

• Product Name: (+)-1,2:5,6-di-O-cyclohexylidene-myo-inositol
• Synonyms: (+)-1,2:5,6-di-O-cyclohexylidene-myo-inositol
• CAS NO: 41545-19-1
• Molecular Weight: 340.417
• Mol File: 41545-19-1.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: (+)-1,2:5,6-di-O-cyclohexylidene-myo-inositol(CAS DataBase Reference)
• NIST Chemistry Reference: (+)-1,2:5,6-di-O-cyclohexylidene-myo-inositol(41545-19-1)
• EPA Substance Registry System: (+)-1,2:5,6-di-O-cyclohexylidene-myo-inositol(41545-19-1)

Safety Data

• Hazardous Substances Data: 41545-19-1(Hazardous Substances Data)

Upstream product

• 933-40-4 cycloxexanone dimethyl ketal 
• 87-89-8 D-myo-inositol 
• 1122-84-5 1-ethoxycyclohexene 
• 6763-47-9 rac-1,2-O-cyclohexylidene-myo-inositol 
• 1670-47-9 1,1-diethoxycyclohexane 
• 101636-71-9 1,6-Di-O-acetyl-2,3:4,5-di-O-cyclohexylidene-D/L-myo-inositol 
• 932-92-3 cyclohexyl ethyl ether 

Downstream Products

• 153996-48-6 2,3:4,5-di-O-cyclohexylidene-1-O-(1R)-menthyloxycarbonyl-D-myo-inositol 
• 124601-98-5 (-)-6-O-benzyl-2,3:4,5-di-O-cyclohexylidene-myo-inositol 
• 40773-58-8 1⁽³⁾-O-benzyl-2,3:4,5-(1,2:5,6)-di-O-cyclohexylidene-myo-inositol 
• 40773-58-8 (+/-)-4-O-benzyl-1,2:5,6-di-O-cyclohexylidene-myo-inositol 
• 40773-58-8 (+/-)-1⁽³⁾-O-benzyl-2,3:4,5-di-O-cyclohexylidene-myo-inositol 
• 13035-68-2 (±)-1,6-di-O-benzyl-2,3:4,5-di-O-cyclohexylidene-myo-inositol 
• 154372-20-0 1D-6-O-allyl-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzoyl)-myo-inositol 
• 211799-72-3 (-)-6-O-allyl-1-O-(p-methoxybenzyl)-2,3-O-cyclohexylidene-myo-inositol 
• 211869-78-2 6-O-allyl-1-O-(p-methoxybenzyl)-2,3:4,5-di-O-cyclohexylidene-myo-inositol 
• 475650-91-0 (+)-6-O-allyl-1-O-(p-methoxybenzyl)-4,5-di-O-benzyl-myo-inositol 
• 475650-90-9 C₃₇H₄₄O₇ 
• 475650-88-5 (-)-2-O-hexadecanoyl-1-O-(p-methoxybenzyl)-3,4,5-tri-O-benzyl-myo-inositol 
• 475650-92-1 (-)-6-O-allyl-2-O-hexadecanoyl-1-O-(p-methoxybenzyl)-3,4,5-tri-O-benzyl-myo-inositol 
• 475650-99-8 6-O-[2-azido-3,6-di-O-benzyl-2-deoxy-4-O-(2-propenyl)-α-D-glucopyranosyl]-2-O-hexadecanoyl-1-O-(p-methoxybenzyl)-3,4,5-tri-O-benzyl-myo-inositol 

Relevant articles and documents

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

Mycothiol cysteine ligase (MshC) is a key enzyme in the mycothiol (MSH) biosynthesis and a promising target for developing new anti-mycobacterial compounds. Herein, we report on the synthesis of substrate analogues, as potential inhibitors, for the MshC e

Synthesis of high-performance polyurethanes with rigid 5-6-5-fused ring system in the main chain from naturally occurring myo-inositol

A bisketal of myo-inositol was used as a diol-type monomer for synthesis of polyurethanes. The monomer was obtained by treatment of myo-inositol with 1,1-dimethoxycyclohexane in the presence of p-toluenesulfonic acid as a catalyst. The ketalization resulted in the formation of a 5-6-5-fused ring system, which endowed the diol-type monomer with high rigidity. The diol readily reacted with diisocyanate to give the corresponding polyurethane, which exhibited excellent heat resistance due to the rigid 5-6-5 system in the main chain. Copyright

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.