55706-57-5 Usage
General Description
6-Methylquinoline-8-carboxylic acid is a chemical compound with the molecular formula C12H9NO2. It is a derivative of quinoline and contains a carboxylic acid group. 6-Methylquinoline-8-carboxylic acid has been used in the synthesis of various pharmaceuticals and agrochemicals due to its potential biological activities. It has also been studied for its antitumor and anti-inflammatory properties. Additionally, 6-Methylquinoline-8-carboxylic acid has been investigated for its potential use as a fluorescent probe for detecting metal ions in biological samples. Overall, this compound has shown promise for various applications in the fields of medicine, agriculture, and analytical chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 55706-57-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,0 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 55706-57:
(7*5)+(6*5)+(5*7)+(4*0)+(3*6)+(2*5)+(1*7)=135
135 % 10 = 5
So 55706-57-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO2/c1-7-5-8-3-2-4-12-10(8)9(6-7)11(13)14/h2-6H,1H3,(H,13,14)
55706-57-5Relevant articles and documents
Development and Mechanistic Study of Quinoline-Directed Acyl C-O Bond Activation and Alkene Oxyacylation Reactions
Hoang, Giang T.,Walsh, Dylan J.,McGarry, Kathryn A.,Anderson, Constance B.,Douglas, Christopher J.
, p. 2972 - 2983 (2017/03/23)
The intramolecular addition of both an alkoxy and acyl substituent across an alkene, oxyacylation of alkenes, using rhodium catalyzed C-O bond activation of an 8-quinolinyl ester is described. Our unsuccessful attempts at intramolecular carboacylation of ketones via C-C bond activation ultimately informed our choice to pursue and develop the intramolecular oxyacylation of alkenes via quinoline-directed C-O bond activation. We provide a full account of our catalyst discovery, substrate scope, and mechanistic experiments for quinoline-directed alkene oxyacylation.
