634-39-9 Usage
Uses
Used in Pharmaceutical Industry:
5-Quinolinecarboxylic acid, 2-methyl-(8CI,9CI) is used as an intermediate in the synthesis of various pharmaceuticals for its potential biological activities. It serves as a key building block in the development of new drugs targeting a range of health conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 5-Quinolinecarboxylic acid, 2-methyl-(8CI,9CI) is utilized as a precursor in the production of agrochemicals, contributing to the development of pesticides and other agricultural chemicals that enhance crop protection and yield.
Used in Biological Research:
5-Quinolinecarboxylic acid, 2-methyl-(8CI,9CI) is employed in biological research as a compound with potential antitumor and anti-inflammatory properties. Its study aids in understanding its mechanism of action and possible applications in therapeutics.
Used in Chemical Synthesis:
As a chemical compound with unique structural features, 5-Quinolinecarboxylic acid, 2-methyl-(8CI,9CI) is used in chemical synthesis for creating a variety of organic compounds and materials, expanding its applications beyond the pharmaceutical and agrochemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 634-39-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,3 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 634-39:
(5*6)+(4*3)+(3*4)+(2*3)+(1*9)=69
69 % 10 = 9
So 634-39-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO2/c1-7-5-6-8-9(11(13)14)3-2-4-10(8)12-7/h2-6H,1H3,(H,13,14)
634-39-9Relevant academic research and scientific papers
PDE 10a Inhibitors for the Treatment of Type II Diabetes
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Paragraph 0979; 0980, (2015/01/06)
Disclosed are compounds, compositions and methods for treating Type II diabetes. Such compounds are represented by Formula (I) as follows: wherein R1, R2, L, and Q are defined herein.
Investigating the antiproliferative activity of quinoline-5,8-diones and styrylquinolinecarboxylic acids on tumor cell lines
Podeszwa,Niedbala,Polanski,Musiol,Tabak,Finster,Serafin,Milczarek,Wietrzyk,Boryczka,Mol,Jampilek,Dohnal,Kalinowski,Richardson
, p. 6138 - 6141 (2008/03/11)
The structure-activity relationships of new quinoline based compounds were investigated. Quinoline-5,8-dione and styrylquinoline scaffolds were used for the design of potentially active compounds. The novel analogues had comparable antiproliferative activ
MUSCARINIC ACETYLCHOLINE RECEPTOR ANTAGONISTS
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Page/Page column 16, (2008/06/13)
Muscarinic Acetylcholine receptor antagonists and methods of using them are provided.
Use of the Kohonen neural network for rapid screening of ex vivo anti-HIV activity of styrylquinolines
Polanski, Jaroslaw,Zouhiri, Fatima,Jeanson, Laurence,Desma?le, Didier,D'Angelo, Jean,Mouscadet, Jean-Fran?ois,Gieleciak, Rafal,Gasteiger, Johann,Le Bret, Marc
, p. 4647 - 4654 (2007/10/03)
Using the Kohonen neural network, the electrostatic potentials on the molecular surfaces of 14 styrylquinoline derivatives were drawn as comparative two-dimensional maps and compared with their known human immunodeficiency virus (HIV)-1 replication blocki
