6739-34-0

Basic information

• Product Name: propyl cyclohexanecarboxylate
• Synonyms: propyl cyclohexanecarboxylate;CYCLOHEXANECARBOXYLIC ACID, PROPYL ESTER;Ai3-19657;Einecs 229-798-0
• CAS NO: 6739-34-0
• Molecular Formula: C₁₀H₁₈O₂
• Molecular Weight: 170.24872
• EINECS: 229-798-0
• Mol File: 6739-34-0.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 215.5°C (estimate)
• Flash Point: 78°C
• Appearance: /
• Density: 0.9530
• Vapor Pressure: 0.152mmHg at 25°C
• Refractive Index: 1.4486 (estimate)
• CAS DataBase Reference: propyl cyclohexanecarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: propyl cyclohexanecarboxylate(6739-34-0)
• EPA Substance Registry System: propyl cyclohexanecarboxylate(6739-34-0)

Safety Data

• Hazardous Substances Data: 6739-34-0(Hazardous Substances Data)

Usage

General Description

Propyl cyclohexanecarboxylate is a chemical compound with the molecular formula C11H20O2. It is an ester, which means it is formed from the reaction of a carboxylic acid and an alcohol. propyl cyclohexanecarboxylate is often used as a flavoring agent in the food industry, particularly in the production of fruit-flavored products such as candies, beverages, and baked goods. It has a sweet, fruity odor and is commonly described as having a tropical, pineapple-like aroma. In addition to its use in the food industry, propyl cyclohexanecarboxylate is also utilized in the manufacturing of perfumes and personal care products for its pleasant fragrance. Overall, this chemical compound plays a key role in enhancing the sensory experience of various consumer products.

InChI:InChI=1/C10H18O2/c1-2-8-12-10(11)9-6-4-3-5-7-9/h9H,2-8H2,1H3

Upstream product

• 71-23-8 propan-1-ol 
• 98-89-5 Cyclohexanecarboxylic acid 
• 110-83-8 cyclohexene 
• 2315-68-6 propyl benzoate 
• 1122-56-1 cyclohexylcarboxamide 
• 136-01-6 cyclohexanecarboxylic acid Na-salt 
• 106-94-5 propyl bromide 
• 100-09-4 4-methoxybenzoic acid 
• 4630-82-4 methyl cyclohexylcarboxylate 

Downstream Products

• 1200437-03-1 1-(2-ethyl-butyl)-cyclohexanecarboxylic acid n-propyl ester 

Relevant articles and documents

Aromatic compound hydrogenation and hydrodeoxygenation method and application thereof

The invention belongs to the technical field of medicines, and discloses an aromatic compound hydrogenation and hydrodeoxygenation method under mild conditions and application of the method in hydrogenation and hydrodeoxygenation reactions of the aromatic compounds and related mixtures. Specifically, the method comprises the following steps: contacting the aromatic compound or a mixture containing the aromatic compound with a catalyst and hydrogen with proper pressure in a solvent under a proper temperature condition, and reacting the hydrogen, the solvent and the aromatic compound under the action of the catalyst to obtain a corresponding hydrogenation product or/and a hydrodeoxygenation product without an oxygen-containing substituent group. The invention also discloses specific implementation conditions of the method and an aromatic compound structure type applicable to the method. The hydrogenation and hydrodeoxygenation reaction method used in the invention has the advantages of mild reaction conditions, high hydrodeoxygenation efficiency, wide substrate applicability, convenient post-treatment, and good laboratory and industrial application prospects.

Combined catalytic system of scandium triflate and boronic ester for amide bond cleavage

We have found that the combination of scandium with boronic ester enables the cleavage of amide bonds. Primary amides were converted to the corresponding esters in the presence of catalytic amounts of scandium triflate and boronic ester under mild and neutral conditions. This unique catalytic system can be applied to the deprotection of acetylaniline derivatives. In addition, control NMR experiments were carried out to examine the effect of the boronic esters. Copyright

NOVEL PROCESS

The present invention relates to a process for the preparation of 1-(2-ethyl-butyl)-cyclohexanecarboxylic acid which is useful as an intermediate in the preparation of pharmaceutically active compounds.