22597-23-5

Basic information

• Product Name: 4-METHYLCYCLOHEXANOL ACETATE
• Synonyms: 4-METHYLCYCLOHEXANOL ACETATE;4-Methylcyclohexyl acetate
• CAS NO: 22597-23-5
• Molecular Formula: C₉H₁₆O₂
• Molecular Weight: 156.22
• Mol File: 22597-23-5.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 191.7°Cat760mmHg
• Flash Point: 66.3°C
• Appearance: /
• Density: 0.95g/cm³
• CAS DataBase Reference: 4-METHYLCYCLOHEXANOL ACETATE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-METHYLCYCLOHEXANOL ACETATE(22597-23-5)
• EPA Substance Registry System: 4-METHYLCYCLOHEXANOL ACETATE(22597-23-5)

Safety Data

• Hazardous Substances Data: 22597-23-5(Hazardous Substances Data)

Usage

General Description

4-Methylcyclohexanol acetate is a chemical compound that belongs to the class of cycloalkanols and their derivatives. It is primarily used as a fragrance ingredient in perfumes, cleaning products, and personal care items. This colorless liquid has a pleasant fruity odor and is known for its sweet and floral aroma. It is commonly used in the fragrance industry due to its ability to enhance the overall scent profile of a product. Additionally, it is also used in the synthesis of other organic compounds. However, 4-Methylcyclohexanol acetate should be handled with care as it may cause irritation to the skin, eyes, and respiratory system if not used properly.

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 

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.