36263-61-3 Usage
Uses
Used in Pharmaceutical Industry:
1-(3-METHOXYPHENYL)-CYCLOHEXANECARBOXYLIC ACID is used as a potential therapeutic agent for its anti-inflammatory and analgesic properties. It is being investigated for its potential to alleviate pain and reduce inflammation in various conditions, making it a valuable asset in the development of new medications for these purposes.
Used in Research and Development:
1-(3-METHOXYPHENYL)-CYCLOHEXANECARBOXYLIC ACID serves as a subject of interest in the field of pharmaceutical research and development. Its potential pharmacological activities, including anti-inflammatory and analgesic properties, make it a valuable compound for further investigation and exploration of its possible applications in the treatment of various medical conditions.
Used in Drug Discovery:
As a compound with potential pharmacological activity, 1-(3-METHOXYPHENYL)-CYCLOHEXANECARBOXYLIC ACID is used in drug discovery efforts to identify new therapeutic agents. Its unique structure and properties may lead to the development of novel drugs for the treatment of pain, inflammation, and other related conditions, contributing to the advancement of medical treatments and patient care.
Check Digit Verification of cas no
The CAS Registry Mumber 36263-61-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,2,6 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 36263-61:
(7*3)+(6*6)+(5*2)+(4*6)+(3*3)+(2*6)+(1*1)=113
113 % 10 = 3
So 36263-61-3 is a valid CAS Registry Number.
36263-61-3Relevant academic research and scientific papers
Meta, para and ortho double exo nucleophilic additions of trimethylsilylester enolates derived from saturated and unsaturated carboxylic acids to tricarbonylchromium complexes of aryl ethers: dearomatizing cyclization to lactones
Rudler, Henri,Comte, Virginie,Garrier, Eva,Bellassoued, Moncef,Chelain, Evelyne,Vaissermann, Jaqueline
, p. 284 - 298 (2007/10/03)
Potassium enolates derived from saturated and unsaturated bis(trimethylsilyl) ketene acetals react with tricarbonylchromium complexes of anisole and diphenylether to give, in addition to α-arylcarboxylic acids, the mono addutcts, lactones, arising from a double exo nucleophilic addition. The latter were not observed in the case of benzenetricarbonylchromium. The intermediate dienol ethers could be isolated and fully characterized by X-ray crystallography. The influenece of the nature of the substituents on the ketene acetals, of the nature of the oxidant, and of the nature of the ester enolates on the course of the reaction has been established and will be discussed.
