36926-83-7 Usage
Uses
Used in Pharmaceutical Industry:
2-Amino-quinoline-3-carboxylic acid ethyl ester is used as a key intermediate in the synthesis of various pharmaceuticals. Its antiproliferative properties make it a promising candidate for the development of cancer treatment drugs. It can be utilized in the creation of novel therapeutic agents that target and inhibit the growth of cancer cells.
Used in Agrochemical Industry:
In the agrochemical sector, 2-amino-quinoline-3-carboxylic acid ethyl ester is used as a precursor in the synthesis of various agrochemicals. Its antimicrobial properties can be harnessed to develop pesticides and fungicides that protect crops from diseases and pests, thereby improving agricultural productivity.
Used in Anti-inflammatory Applications:
Due to its anti-inflammatory properties, 2-amino-quinoline-3-carboxylic acid ethyl ester can be employed in the development of anti-inflammatory drugs. These drugs can help alleviate inflammation and pain associated with various conditions, such as arthritis, allergies, and other inflammatory disorders.
Used in Antimicrobial Applications:
The antimicrobial properties of 2-amino-quinoline-3-carboxylic acid ethyl ester make it suitable for use in the development of antimicrobial agents. These agents can be used in various applications, such as disinfectants, sanitizers, and preservatives, to combat the growth of harmful microorganisms and maintain hygiene in various settings, including healthcare, food processing, and personal care products.
Check Digit Verification of cas no
The CAS Registry Mumber 36926-83-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,9,2 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 36926-83:
(7*3)+(6*6)+(5*9)+(4*2)+(3*6)+(2*8)+(1*3)=147
147 % 10 = 7
So 36926-83-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H12N2O2/c1-2-16-12(15)9-7-8-5-3-4-6-10(8)14-11(9)13/h3-7H,2H2,1H3,(H2,13,14)
36926-83-7Relevant academic research and scientific papers
Copper-catalyzed synthesis of quinoline derivatives via tandem Knoevenagel condensation, amination and cyclization
Dhiman, Shiv,Saini, Hitesh Kumar,Nandwana, Nitesh Kumar,Kumar, Dalip,Kumar, Anil
, p. 23987 - 23994 (2016/03/15)
A novel regioselective synthesis of 2-aminoquinolines and 2-arylquinoline-3-carbonitriles is described via copper-mediated tandem reaction. Formation of substituted quinolines involves Knoevenagel condensation of ortho-bromobenzaldehyde with active methylene nitriles followed by copper-catalyzed reductive amination and intramolecular cyclization.
