2611-02-1 Usage
Description
Cyclohexylmethyl cyclohexanecarboxylate is an organic compound that belongs to the class of esters. It is characterized by its unique chemical structure, which consists of a cyclohexane ring with a cyclohexylmethyl group attached to the ester functional group. cyclohexylmethyl cyclohexanecarboxylate is known for its versatile chemical properties and potential applications in various industries.
Uses
Used in Synthetic Chemistry:
Cyclohexylmethyl cyclohexanecarboxylate is used as a synthetic intermediate for the preparation of various esters. It plays a crucial role in the iodine-mediated oxidative condensation of alcohols, a reaction that allows for the formation of new ester compounds with potential applications in different fields.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, cyclohexylmethyl cyclohexanecarboxylate is used as a key component in the synthesis of drug molecules. Its unique structure and reactivity make it a valuable building block for the development of new pharmaceutical agents with potential therapeutic benefits.
Used in Fragrance Industry:
Cyclohexylmethyl cyclohexanecarboxylate is also used in the fragrance industry as a component in the creation of various scent compounds. Its unique aroma profile contributes to the development of new and innovative fragrances for a wide range of applications, including perfumes, cosmetics, and personal care products.
Used in Flavor Industry:
In the flavor industry, cyclohexylmethyl cyclohexanecarboxylate is employed as a flavoring agent. Its distinct taste profile can be used to enhance the flavor of various food and beverage products, contributing to a more diverse and enjoyable taste experience for consumers.
Used in Material Science:
Cyclohexylmethyl cyclohexanecarboxylate has potential applications in material science, particularly in the development of new polymers and materials with unique properties. Its chemical structure and reactivity can be utilized to create novel materials with improved performance characteristics for various applications, such as coatings, adhesives, and plastics.
Synthesis Reference(s)
The Journal of Organic Chemistry, 52, p. 4319, 1987 DOI: 10.1021/jo00228a032Tetrahedron Letters, 28, p. 6229, 1987 DOI: 10.1016/S0040-4039(00)61854-3
Check Digit Verification of cas no
The CAS Registry Mumber 2611-02-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,1 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2611-02:
(6*2)+(5*6)+(4*1)+(3*1)+(2*0)+(1*2)=51
51 % 10 = 1
So 2611-02-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H24O2/c15-14(13-9-5-2-6-10-13)16-11-12-7-3-1-4-8-12/h12-13H,1-11H2
2611-02-1Relevant articles and documents
Metal complex catalysts and method for catalytically reducing carboxylic acids
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Paragraph 0156; 0165; 0166; 0178-0179, (2020/06/20)
The invention relates to a metal complex catalyst, which contains at least one of metal complexes with a chemical formula comprising a structural unit represented by a formula I. According to the invention, the center metal of the metal complex catalyst is iridium, and the metal complex catalyst is composed of pentamethylcyclopentadienyl, a bitetrahydropyrimidine ligand and proper coordination anions; the metal complex catalyst has activity on a carboxylic acid reduction reaction, and a carboxylic acid compound is reduced into an alcohol compound in the presence of hydrogen; and the method ismild in reaction condition, can be carried out at room temperature, and is good in catalytic performance and high in reduction product yield.
Pd-Catalyzed Dehydrogenative Oxidation of Alcohols to Functionalized Molecules
Mori, Takamichi,Ishii, Chihiro,Kimura, Masanari
supporting information, p. 1709 - 1717 (2019/09/04)
A dehydrogenative oxidation reaction of primary alcohols to aldehydes catalyzed by a simple Pd/Xantphos catalytic system was developed under an argon or nitrogen atmosphere without oxidizing agents or hydrogen acceptors. The reaction product could be easily changed: under aerobic conditions, esters were obtained in aprotic solvents, whereas the corresponding carboxylic acids were produced in aqueous media. These oxidizing processes were applicable to the efficient synthesis of useful nitrogen-containing heterocyclic compounds such as indole, quinazoline, and benzimidazole via intramolecular versions of this reaction from amino alcohols.
Oxidative esterification of primary alcohols at room temperature under aqueous medium
Reddy, N. Naresh Kumar,Ravi, Chitrakar,Adimurthy, Subbarayappa
, p. 1663 - 1670 (2018/06/15)
Oxidative esterification of aliphatic primary alcohols with bromide and bromate couple in aqueous acidic medium at room temperature is reported with a wide range of substrate scope for both aliphatic and cyclic alcohols and obtained excellent yields of products.
