6848-53-9

Basic information

• Product Name: 1 2:3 4-DI-O-CYCLOHEXYLIDENE-5-O-METHYL&
• Synonyms: 1 2:3 4-DI-O-CYCLOHEXYLIDENE-5-O-METHYL&
• CAS NO: 6848-53-9
• Molecular Formula: C₁₉H₃₀O₆
• Molecular Weight: 354.44
• Product Categories: Carbohydrate Synthesis;Monosaccharides;Specialty Synthesis
• Mol File: 6848-53-9.mol
• Article Data: 4

Chemical Properties

• Melting Point: 121-124 °C(lit.)
• Boiling Point: 517.8±50.0 °C(Predicted)
• Appearance: /
• Density: 1.26±0.1 g/cm3(Predicted)
• PKA: 13.13±0.40(Predicted)
• CAS DataBase Reference: 1 2:3 4-DI-O-CYCLOHEXYLIDENE-5-O-METHYL&(CAS DataBase Reference)
• NIST Chemistry Reference: 1 2:3 4-DI-O-CYCLOHEXYLIDENE-5-O-METHYL&(6848-53-9)
• EPA Substance Registry System: 1 2:3 4-DI-O-CYCLOHEXYLIDENE-5-O-METHYL&(6848-53-9)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 6848-53-9(Hazardous Substances Data)

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

• 157727-65-6 1-O-benzoyl-3,4:5,6-di-O-cyclohexylidene-2-O-methyl-(-)-chiro-inositol 
• 6763-54-8 1L-1,2:3,4-di-O-cyclohexylidene-5-O-methyl-6-O-(p-tolylsulfonyl)-chiro-inositol 
• 60504-85-0 1L-1-O-benzoyl-3,4:5,6-di-O-cyclohexylidene-2-O-methyl-chiro-inositol 
• 725273-54-1 1-O-benzoyl-2-O-methyl-(-)-chiro-inositol 
• 17230-42-1 3,4,5,6-Tetra-O-methyl-(-)-inosit; L-(1,2,4-3,5,6)-3,4,5,6-Tetramethoxy-1,2-cyclohexandiol 
• 117708-51-7 ((1R,2S,3S,4R,5S,6R)-2,3,4,5,6-Pentamethoxy-cyclohexyloxymethyl)-benzene 
• 402832-38-6 L-1-O-benzyl-2-O-methyl-chiro-inositol 
• 754197-60-9 (2S,3R,4S,5S,6S)-2-Benzyloxy-3,4,5,6-tetramethoxy-cyclohexanone 
• 755024-66-9 ((2R,3S,5S,6R)-2,3,4,5,6-Pentamethoxy-cyclohexyloxymethyl)-benzene 
• 754197-59-6 (1R,2R,3R,4S,5R,6R)-2-Benzyloxy-3,4,5,6-tetramethoxy-cyclohexanol 
• 754197-62-1 (1S,2R,3R,4S,5R,6R)-2-Benzyloxy-3,4,5,6-tetramethoxy-cyclohexanol 
• 754197-54-1 (1R,2S,3S,4S,5S,6S)-5-Benzyloxy-6-methoxy-cyclohexane-1,2,3,4-tetraol 
• 754197-53-0 C₂₆H₃₆O₆ 
• 152884-28-1 (1R,2R,3S,4R,5R)-1-O-(methyl)cyclohexane-1,2,3,4,5-pentol 

Relevant articles and documents

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.

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.