716361-84-1 Usage
Carboxylic acid
It is a type of organic compound that contains a carboxyl group (-COOH), which gives it acidic properties.
Cyclohexane ring
The compound contains a six-membered carbon ring with alternating single and double bonds, which is characteristic of cyclohexane structures.
Phenoxy group
A phenol group (-OH attached to a benzene ring) is attached to the cyclohexane ring, forming a phenoxy group. This contributes to the compound's unique chemical properties.
Building block in synthesis
1-phenoxy-cyclohexanecarboxylic acid is commonly used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, making it an important compound in the chemical industry.
Anti-inflammatory properties
The compound has been studied for its potential to reduce inflammation, which could make it useful in the development of new anti-inflammatory medications.
Antioxidant properties
1-phenoxy-cyclohexanecarboxylic acid has also been investigated for its potential antioxidant properties, which could help protect cells from damage caused by free radicals.
Ongoing scientific research
1-phenoxy-cyclohexanecarboxylic acid continues to be a topic of interest in scientific research, as its various properties and potential applications are further explored and developed.
Check Digit Verification of cas no
The CAS Registry Mumber 716361-84-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,1,6,3,6 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 716361-84:
(8*7)+(7*1)+(6*6)+(5*3)+(4*6)+(3*1)+(2*8)+(1*4)=161
161 % 10 = 1
So 716361-84-1 is a valid CAS Registry Number.
716361-84-1Relevant articles and documents
KF-alumina-mediated Bargellini reaction
Rohman, Md. Rumum,Myrboh, Bekington
experimental part, p. 4772 - 4775 (2010/09/20)
KF-alumina was found to be an efficient base for the synthesis of sterically hindered α-substituted carboxylic acids. A series of Bargellini reactions were performed by using various substituted anilines, phenols, and thiophenols as nucleophiles with keto
Potent and selective cathepsin K inhibitors
Shinozuka, Tsuyoshi,Shimada, Kousei,Matsui, Satoshi,Yamane, Takahiro,Ama, Mayumi,Fukuda, Takeshi,Taki, Motohiko,Takeda, Yuko,Otsuka, Eri,Yamato, Michiko,Mochizuki, Shin-ichi,Ohhata, Keiko,Naito, Satoru
, p. 6789 - 6806 (2007/10/03)
A novel series of cathepsin K inhibitors derived from Novartis compound I is described. Optimization of the P1, P3, and P1′ units led to the identification of 4-aminophenoxyacetic acid 24b with an IC50 value of 4.8 nM, which possessed an excell
