6848-53-9

Usage

Uses

Used in Organic Synthesis:
1 2:3 4-DI-O-CYCLOHEXYLIDENE-5-O-METHYL& is used as an intermediate in organic synthesis for its ability to alter the reactivity and physical properties of the fructose molecule. This makes it a valuable compound for developing new materials and organic compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1 2:3 4-DI-O-CYCLOHEXYLIDENE-5-O-METHYL& is used as a key compound in the development of new drugs. Its unique structure and properties allow researchers to explore its potential in creating novel pharmaceuticals with various applications.
Used in Material Science:
1 2:3 4-DI-O-CYCLOHEXYLIDENE-5-O-METHYL& is also used in material science as a component in the creation of new materials. Its modified fructose structure can contribute to the development of advanced materials with specific properties for various applications.

Upstream product

• 1122-84-5 1-ethoxycyclohexene 
• 642-38-6 quebrachitol 
• 108-94-1 cyclohexanone 
• 933-40-4 cycloxexanone dimethyl ketal 

Downstream Products

• 6763-54-8 1L-1,2:3,4-di-O-cyclohexylidene-5-O-methyl-6-O-(p-tolylsulfonyl)-chiro-inositol 
• 157727-65-6 1-O-benzoyl-3,4:5,6-di-O-cyclohexylidene-2-O-methyl-(-)-chiro-inositol 
• 157727-66-7 1L-1-O-benzyl-5,6-O-cyclohexylidene-2-O-methyl-chiro-inositol 
• 157727-68-9 (1R,2S,5R,6R)-5-benzyloxy-6-methoxycyclohex-3-ene-1,2-diyl acetate 
• 157727-67-8 1L-3,4-di-O-acetyl-1-O-benzyl-2-O-methyl-chiro-inositol 
• 166184-28-7 1L-3,4-di-O-acetyl-1-O-benzyl-2-O-methyl-5,6-O-thiocarbonyl-chiro-inositol 
• 166184-27-6 1L-3,4-di-O-acetyl-1-O-benzyl-5,6-O-cyclohexylidene-2-O-methyl-chiro-inositol 
• 52432-16-3 (+)-3-deoxy-3-azido-myo-inositol 
• 488-76-6 (-)-viburnitol 
• 6763-52-6 1L-1-O-(p-tolylsulfonyl)-chiro-inositol 
• 143393-84-4 1D-3-chloro-3-deoxy-myo-inositol 
• 128441-63-4 D-(+)-myo-inositol 1-phosphate bis(cyclohexylammonium) salt 
• 134865-99-9 C₄₁H₃₃O₁₄P 
• 128352-27-2 D-2,3,4,5,6-penta-O-benzoyl-1-O-(o-xylene-α,α'-diyldioxyphosphoryl)-myo-inositol 

Relevant academic research and scientific papers

Improved synthesis of dicyclohexylidene protected quebrachitol and its use in the synthesis of l-chiro-inositol derivatives

A modified synthesis of 1l-1,2:3,4-di-O-cyclohexylidene-5-O-methyl-chiro-inositol has been accomplished that improves the overall procedure, yield, and environmental aspects of its formation. Several inositol analogues have been prepared from this intermediate for testing as biosynthetic inhibitors of glycosyl-phosphatidylinositol (GPI) anchor formation.

Enzyme-catalysed synthesis of galactosylated 1D- and 1L-chiro-inositol, 1D-pinitol, myo-inositol and selected derivatives using the β-galactosidase from the thermophile Thermoanaerobacter sp. strain TP6-B1

The products from the enzymatic β-D-galactopyranosylation of 1D-chiro-inositol, 1D-pinitol, 1D-3-O-allyl-4-O-methyl-chiro-inositol, 1D-3,4-di-O-methyl-chiro-inositol, 1L-chiro-inositol and myo-inositol in combined yields ranging from 46% to 64% have been

Total synthesis of (-)-ovalicin and analogues from L-quebrachitol

We describe here the first chiral total synthesis of (-)-ovalicin and the synthesis of several related analogues, from the naturally occuring cyclitol L-quebrachitol.

Synthesis and evaluation of 3-modified 1D-myo-inositols as inhibitors and substrates of phosphatidylinositol synthase and inhibitors of myo-inositol uptake by cells

A number of 3-substituted 1D-myo-inositols were synthesized and evaluated as substrates for phosphatidylinositol synthase and uptake by intact cells. 1D-3-Amino-, -3-chloro-, and -3-(acetylthio)-3-deoxy-myo-inositols were all synthesized by nucleophilic d