57089-24-4

Basic information

• Product Name: 3,2:1,6-di-O-cyclohexylidene-sn-myoinositol
• Synonyms: 3,2:1,6-di-O-cyclohexylidene-sn-myoinositol
• CAS NO: 57089-24-4
• Molecular Weight: 340.417
• Mol File: 57089-24-4.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 3,2:1,6-di-O-cyclohexylidene-sn-myoinositol(CAS DataBase Reference)
• NIST Chemistry Reference: 3,2:1,6-di-O-cyclohexylidene-sn-myoinositol(57089-24-4)
• EPA Substance Registry System: 3,2:1,6-di-O-cyclohexylidene-sn-myoinositol(57089-24-4)

Safety Data

• Hazardous Substances Data: 57089-24-4(Hazardous Substances Data)

Upstream product

• 932-92-3 cyclohexyl ethyl ether 
• 87-89-8 D-myo-inositol 
• 1670-47-9 1,1-diethoxycyclohexane 
• 1122-84-5 1-ethoxycyclohexene 
• 6763-47-9 rac-1,2-O-cyclohexylidene-myo-inositol 
• 933-40-4 cycloxexanone dimethyl ketal 

Downstream Products

• 124575-20-8 C₄₀H₆₄O₁₀ 
• 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 
• 116096-44-7 C₃₄H₄₄O₈ 
• 101400-45-7 cyklohexylammonium salt of 4⁽⁶⁾,5-bis-O-phospho-sn-myoinositol 
• 115015-97-9 (-)-1L-2,6-di-O-benzyl-myo-inositol 
• 116786-69-7 (+)-3,4-di-O-allyl-5,6-di-O-benzyl-myo-inositol 
• 115509-76-7 (-)-1D-2,5,6-tri-O-benzyl-myo-inositol 
• 140148-49-8 (-)-3,4,5-tri-O-allyl-6-O-benzyl-myo-inositol 
• 117666-31-6 (+)-1,3,4,5-tetra-O-allyl-6-O-benzyl-myo-inositol 
• 139978-97-5 (+)-3,4-di-O-allyl-6-O-benzyl-1,2-O-cyclohexylidene-myo-inositol 
• 145789-54-4 (-)-3,4,5-tri-O-allyl-6-O-benzyl-1,2-O-cyclohexylidene-myo-inositol 
• 140148-51-2 (+)-1,3,4-tri-O-allyl-5,6-di-O-benzyl-myo-inositol 
• 117666-30-5 (+)-1,3,4,5-tetra-O-allyl-2,6-di-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.