42742-00-7

Basic information

• Product Name: Diacetic acid 1α,4α-cyclohexylene ester
• Synonyms: 1,4-Cyclohexanediol, diacetate, cis-;cis-1,4-Diacetoxycyclohexane;Nsc245877
• CAS NO: 42742-00-7
• Molecular Formula: C₁₀H₁₆O₄
• Molecular Weight: 200.23164
• Mol File: 42742-00-7.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 249.7°C at 760 mmHg
• Flash Point: 115.4°C
• Appearance: /
• Density: 1.09g/cm³
• Vapor Pressure: 0.0226mmHg at 25°C
• Refractive Index: 1.457
• CAS DataBase Reference: Diacetic acid 1α,4α-cyclohexylene ester(CAS DataBase Reference)
• NIST Chemistry Reference: Diacetic acid 1α,4α-cyclohexylene ester(42742-00-7)
• EPA Substance Registry System: Diacetic acid 1α,4α-cyclohexylene ester(42742-00-7)

Safety Data

• Hazardous Substances Data: 42742-00-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H16O4/c1-7(11)13-9-3-5-10(6-4-9)14-8(2)12/h9-10H,3-6H2,1-2H3

Upstream product

• 110-82-7 cyclohexane 
• 556-48-9 1,4-Cyclohexanediol 
• 108-24-7 acetic anhydride 
• 931-71-5 cis-1,4-cyclohexanediol 
• 64-19-7 acetic acid 
• 75-36-5 acetyl chloride 
• 637-88-7 1,4-Cyclohexanedione 
• 787-07-5 diethyl 1,4-cyclohexanedione-2,5-dicarboxylate 
• 108-22-5 Isopropenyl acetate 

Downstream Products

• 931-71-5 cis-1,4-cyclohexanediol 
• 72156-95-7 cis-1-Acetoxy-cyclohexanol-⁽⁴⁾ 
• 6995-79-5 cyclohexane-1,4-diol 
• 16890-91-8 trans-1,4-dichlorocyclohexane 
• 13618-83-2 trans-1,4-dibromocyclohexane 

Relevant articles and documents

Process for preparing monoesters

A process for preparing monoesters comprises the step of reacting at least one diol with at least one carboxylic acid in a biphasic solvent system, the carboxylic acid being sufficiently water soluble to allow esterification to occur, and the biphasic solvent system comprising water and at least one aprotic solvent in which the resulting monoester has greater solubility than in water.

Facile and highly selective monoacylation of symmetric diols adsorbed on silica gel with acetyl chloride

Monoacetylated alcohols of symmetric 1,n-diols are synthesized quantitatively by refluxing a suspension of the diols adsorbed on silica gel with acetylchloride.

OXYGENATION OF AROMATIC AND ALIPHATIC HYDROCARBONS BY A NEW REAGENT SYSTEM, Fe(CH3CN)6(2+)-H2O2-Ac2O: AN EFFECTIVE MODEL REAGENT FOR MONO-OXYGENASE

Reactions of aromatic and aliphatic hydrocarbons with a new system, Fe(CH3CN)6(2+) - H2O2 - Ac2O in CH3CN, gave oxygenation products with fairly high reaction efficiency ( Tables I and II )compared to known to reagent systems used as enzyme models for mono-oxygenases.Investigations of the mechanism of these reactions indicated the involvement of either complex C.FeIV(OH)(OAc)(2+), or complex D, FeIV(OAc)(2+), dependig on the organic substrate.Keywords-oxygenation; aromatic hydrocarbon; aliphatic hydrocarbon; hexakisacetonitrile iron(II) perchlorate; hydrogen peroxide; enzyme model; mono-oxygenase