13332-20-2

Basic information

• Product Name: cis-4-methylcyclohexyl acetate
• Synonyms: cis-4-methylcyclohexyl acetate;4-Methylcyclohexylacetate=4MCHA;Aceticacidcis-4-methylcyclohexylester;4α-Methyl-1α-cyclohexanol acetate;Acetic acid 4α-methylcyclohexan-1α-yl ester;Acetic acid 4β-methylcyclohexane-1β-yl ester;Einecs 236-383-8
• CAS NO: 13332-20-2
• Molecular Formula: C₉H₁₆O₂
• Molecular Weight: 156.22214
• EINECS: 236-383-8
• Mol File: 13332-20-2.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Refractive Index: 1.444
• CAS DataBase Reference: cis-4-methylcyclohexyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: cis-4-methylcyclohexyl acetate(13332-20-2)
• EPA Substance Registry System: cis-4-methylcyclohexyl acetate(13332-20-2)

Safety Data

• Hazardous Substances Data: 13332-20-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C9H16O2/c1-7-3-5-9(6-4-7)11-8(2)10/h7,9H,3-6H2,1-2H3/t7-,9+

Upstream product

• 589-91-3 p-methylcyclohexanol 
• 108-24-7 acetic anhydride 
• 64-19-7 acetic acid 
• 108-22-5 Isopropenyl acetate 
• 589-92-4 1-methylcyclohexan-4-one 
• 106-44-5 p-cresol 
• 15876-34-3 trans-4-methylcyclohexyl acetate 
• 108-05-4 vinyl acetate 
• 7731-28-4 cis-4-methylcyclohexanol 

Downstream Products

• 15876-34-3 trans-4-methylcyclohexyl acetate 

Relevant articles and documents

-

-

Solvent-free acetylation and tetrahydropyranylation of alcohols catalyzed by recyclable sulfonated ordered nanostructured carbon

Rapid and practical green acetylation and tetrahydropyranylation routes of structurally diverse alcohols and phenols were applied under solvent-free reaction conditions providing excellent yields, using catalytic amounts of environmentally friendly sulfonated ordered nanoporous carbon (CMK-5-SO 3H). Non-toxic nature of the catalyst, its easy handling, recovery and reusability, and the absence of any solvent characterize the presented procedures as efficient methods. These procedures provide methods for the separation of the product by simple filtration.

Meerwein-Ponndorf-Verley-type reductive acetylation of carbonyl compounds to acetates by lanthanide complexes in the presence of isopropenyl acetate

Meerwein-Ponndorf-Verley-type reductive acetylation of carbonyl compounds to acetates was successfully carried out in the presence of isopropenyl acetate under the influence of a catalytic amount of Ln(O(i)Pr)3 at room temperature. Various carbonyl compounds were converted into the corresponding acetates in fair to good yields. (C) 2000 Elsevier Science Ltd.