25348-62-3

Basic information

• Product Name: 3,4,5,6-TETRA-O-ACETYL-MYO-INOSITOL-1,2-THIOCARBONATE
• Synonyms: 3,4,5,6-TETRA-O-ACETYL-MYO-INOSITOL-1,2-THIOCARBONATE;Myo-Inositol Cyclic 1,2-carbonothioate 3,4,5,6-tetraacetate;OGDPAADFSHXROB-DHRKEOQWSA-N
• CAS NO: 25348-62-3
• Molecular Formula: C₁₅H₁₈O₁₀S
• Molecular Weight: 390.36242
• Product Categories: All Inositols;Inositols;Intermediates & Fine Chemicals;Pharmaceuticals
• Mol File: 25348-62-3.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 420.5±55.0 °C(Predicted)
• Appearance: /
• Density: 1.43±0.1 g/cm3(Predicted)
• Storage Temp.: Refrigerator
• Solubility: Chloroform, Dichloromethane, Ethyl Acetate
• CAS DataBase Reference: 3,4,5,6-TETRA-O-ACETYL-MYO-INOSITOL-1,2-THIOCARBONATE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4,5,6-TETRA-O-ACETYL-MYO-INOSITOL-1,2-THIOCARBONATE(25348-62-3)
• EPA Substance Registry System: 3,4,5,6-TETRA-O-ACETYL-MYO-INOSITOL-1,2-THIOCARBONATE(25348-62-3)

Safety Data

• Hazardous Substances Data: 25348-62-3(Hazardous Substances Data)

Usage

Chemical Properties

White Solid

Uses

3,4,5,6-Tetra-O-acetyl myo-Inositol-1,2-thiocarbonate is used in the synthesis of Conduritol B epoxide.

Upstream product

• 87-89-8 D-myo-inositol 
• 39110-61-7 3,4,5,6-tetra-O-acetyl-1,2-O-cyclohexylidene-myo-inositol 
• 463-71-8 thiophosgene 
• 13462-79-8 1⁽³⁾,4⁽⁶⁾,5,6⁽⁴⁾-tetra-O-acetyl-sn-myo-inositol 
• 6160-65-2 1,1'-Thiocarbonyldiimidazole 

Downstream Products

• 135346-51-9 Acetic acid (1S,2S,5R,6S)-5,6-diacetoxy-2-(2,2-dimethyl-4,6-dioxo-[1,3]dioxan-5-yl)-cyclohex-3-enyl ester 
• 135346-53-1 ((1S,4S,5R,6R)-4,5,6-Triacetoxy-cyclohex-2-enyl)-acetic acid 2-thioxo-2H-pyridin-1-yl ester 
• 69982-91-8 (1SR,2RS,3SR,6RS)-1,2,3-triacetoxy-6-(acetoxymethyl)cyclohex-4-ene 
• 135346-52-0 ((1S,4S,5R,6R)-4,5,6-Triacetoxy-cyclohex-2-enyl)-acetic acid 
• 4381-96-8 (+/-)-(1,3/2,4)-1,2,3,4-tetra-O-acetyl-5-cyclohexene-1,2,3,4-tetrol 
• 6090-95-5 conduritol β-epoxide 
• 526-87-4 (+/-)-Conduritol B 

Relevant articles and documents

SYNTHESIS OF BRANCHED-CHAIN CYCLITOLS USING A PALLADIUM(0)-CATALYZED ALLYLIC COUPLING REACTION

A carbanion derived from Meldrum's acid was used in a palladium(0)-catalysed allylic substitution reaction to prepare stereospecifically branched-chain cyclitols from the symmetrical 1,2,3,4-tetraacetoxycyclohex-5-ene (4).