55123-26-7

Basic information

• Product Name: 1,2:4,5-DI-O-CYCLOHEXYLIDENE-MYO-INOSITOL
• Synonyms: 1,2:4,5-Biscyclohexylidene D-Myo-Inositol;1,2:4,5-Di-O-cyclohexylidene-
• CAS NO: 55123-26-7
• Molecular Formula: C₁₈H₂₈O₆
• Molecular Weight: 340.413
• Product Categories: Carbohydrates & Derivatives;Inositols
• Mol File: 55123-26-7.mol
• Article Data: 17

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,2:4,5-DI-O-CYCLOHEXYLIDENE-MYO-INOSITOL(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2:4,5-DI-O-CYCLOHEXYLIDENE-MYO-INOSITOL(55123-26-7)
• EPA Substance Registry System: 1,2:4,5-DI-O-CYCLOHEXYLIDENE-MYO-INOSITOL(55123-26-7)

Safety Data

• Hazardous Substances Data: 55123-26-7(Hazardous Substances Data)

Usage

Description

1,2:4,5-Di-O-cyclohexylidene-myo-inositol is a chemical compound derived from myo-inositol, a naturally occurring carbohydrate found in many living organisms. It is characterized by the presence of two cyclohexylidene groups at the 1,2 and 4,5 positions, which protect the hydroxyl groups and facilitate its use in various chemical reactions and applications.

Uses

Used in Biochemical Studies:
Used in Pharmaceutical Industry:
1,2:4,5-Di-O-cyclohexylidene-myo-inositol is used as a key building block for the development of novel pharmaceutical compounds targeting inositol-binding proteins. These proteins are involved in various signaling pathways and have been implicated in a range of diseases, making them attractive targets for drug discovery efforts.
Used in Chemical Synthesis:
1,2:4,5-Di-O-cyclohexylidene-myo-inositol is used as a versatile starting material for the synthesis of various inositol-based compounds with potential applications in different industries, such as pharmaceuticals, agrochemicals, and materials science. The cyclohexylidene protection groups allow for selective functionalization and modification of the inositol core, enabling the creation of a diverse range of derivatives with tailored properties and applications.

Upstream product

• 129094-32-2 1,2;4,5-Di-O-cyclohexylidene-3-O-trifluoromethanesulfonyl-myo-inositol 
• 134109-13-0 D-3-O-benzoyl-1,2:4,5-di-O-cyclohexylidene-myo-inositol 
• 126647-64-1 2,3:5,6-(1,2:4,5)-dicyclohexylidene-myo-inositol 1,4-(3,6)-biscamphanate 
• 932-92-3 cyclohexyl ethyl ether 
• 87-89-8 D-myo-inositol 
• 126647-64-1 2,3:5,6-(1,2:4,5)-dicyclohexylidene-myo-inositol 1,4-(3,6)-biscamphanate 
• 111901-83-8 6-O-Camphanoyl-1,2;4,5-di-O-cyclohexylidene-3-O-benzyl-D-myo-inositol 
• 132891-77-1 6-O-Camphanoyl-1,2;4,5-di-O-cyclohexylidene-D-myo-inositol 
• 801301-07-5 L-3,6-di-O-[(S)-O-acetylmandeloyl]-1,2-O-cyclohexylidene-myo-inositol 
• 111828-85-4 6-O-Camphanoyl-1,2;4,5-di-O-cyclohexylidene-3-O-benzyl-L-myo-inositol 
• 132891-77-1 6-O-Camphanoyl-1,2;4,5-di-O-cyclohexylidene-L-myo-inositol 
• 801301-08-6 D-3,6-di-O-[(S)-O-acetylmandeloyl]-1,2-O-cyclohexylidene-myo-inositol 
• 1122-84-5 1-ethoxycyclohexene 
• 129115-29-3 6-O-Camphanoyl-1,2;4,5-di-O-cyclohexylidene-3-O-trifluoromethanesulfonyl-D-myo-inositol 

Downstream Products

• 141033-52-5 C₃₄H₄₄BrO₉P 
• 34361-60-9 D-1,2:4,5-di-O-cyclohexylidene-myo-inositol 
• 34361-60-9 1L-1,2:4,5-di-O-cyclohexylidene-myo-inositol 
• 26277-05-4 1,2,4,5,6-penta-O-benzyl-sn-myo-inositol 
• 131146-91-3 (+/-)-4-O-allyl-1,5,6-tri-O-benzyl-myo-inositol 
• 114218-29-0 1L-1-O-allyl-2,3,4,5,6-penta-O-benzyl-myo-inositol 
• 136282-32-1 6-O-allyl-3-O-benzyl-1,2-O-cyclohexylidene-myo-inositol 
• 134039-17-1 C₂₃H₃₂O₇ 
• 136282-38-7 1,4-di-O-allyl-5,6-di-O-benzyl-3-O-tert-butyldimethylsilyl-myo-inositol 
• 129879-49-8 6-O-allyl-3-O-benzyl-1,2:4,5-di-O-cyclohexylidene-myo-inositol 
• 134039-19-3 (1R,2S,3S,4R,5R,6S)-3-Allyloxy-4,5-bis-benzyloxy-6-(4-methoxy-benzyloxy)-cyclohexane-1,2-diol 
• 134039-16-0 C₂₉H₄₀O₇ 
• 136282-40-1 2,5,6-tri-O-benzyl-1,4-di-O-trans-prop-1-enyl-myo-inositol 
• 136282-33-2 4-O-allyl-1,5,6-tri-O-benzyl-3-O-tert-butyldimethylsilyl-myo-inositol 

Relevant articles and documents

Design and synthesis of biotinylated inositol phosphates relevant to the biotin-avidin techniques

Six bifunctional molecules containing biotin and various inositol phosphates were synthesized. These compounds were designed on the basis of X-ray structures of the complexes of d-myo-inositol 1,4,5-triphosphates (IP 3) and phospholipase C δ pleckstrin homology domain (PLCδ PH) considering the application to the biotin-avidin techniques. The building blocks of the inositol moiety were synthesized starting with optically resolved myo-inositol derivatives and assembled to the biotin linker through a phosphate linkage. The Royal Society of Chemistry.

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 mycothiol, 1D-1-O-(2-[N-acetyl-L-cysteinyl]amino-2-deoxy-α-D-glucopyranosyl)-myo-inositol, principal low molecular mass thiol in the actinomycetes

Members of the actinomycetes produce 1D-1-O-(2-[N-acetyl-l-cysteinyl]amino-2-deoxy-α-D-glucopyranosyl)-myo-inositol or mycothiol 1 as principal low molecular mass thiol. Chemical synthesis of a biosynthetic precursor of mycothiol, the pseudo-disaccharide