20146-24-1 Usage
General Description
2-(2-FURYL)-6-METHYLQUINOLINE-4-CARBOXYLIC ACID is a chemical compound that belongs to the quinoline family. It is a derivative of quinoline with a furan group at the 2-position and a carboxylic acid group at the 4-position. 2-(2-FURYL)-6-METHYLQUINOLINE-4-CARBOXYLIC ACID has potential applications in the pharmaceutical industry as it exhibits various biological activities, including antimicrobial, antifungal, and anti-inflammatory properties. It can also be used as a building block in the synthesis of other organic compounds. Additionally, 2-(2-FURYL)-6-METHYLQUINOLINE-4-CARBOXYLIC ACID may have potential use as a fluorescent probe in biochemical and biomedical research.
Check Digit Verification of cas no
The CAS Registry Mumber 20146-24-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,4 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 20146-24:
(7*2)+(6*0)+(5*1)+(4*4)+(3*6)+(2*2)+(1*4)=61
61 % 10 = 1
So 20146-24-1 is a valid CAS Registry Number.
20146-24-1Relevant articles and documents
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Ardasev,Gajdzurova
, (1968)
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Synthesis, characterization and antibacterial activities of some N-bridged heterocycles containing triazole, quinoline and nitrofuran moieties
Holla, B. Shivarama,Shridhara,Rao, B. Sooryanarayana,Poojary, K. Narayana
, p. 105 - 109 (2007/10/03)
A series of 2-(2-furyl)4-quinolinecarboxylic acids (3), 2-(5-nitro-2-furyl)4-quinolinecarboxylic acids (6), 4-(3-aryloxymethyl-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazolo-6-yl)-2- (furyl)quinolines (5) and 4-(3-aryloxymethyl-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazolo-6-yl)-2- (5-nitro-2-furyl)quinolines (7) were synthesized. The structures of the newly synthesized compounds are confirmed on the basis of elemental analysis, IR, 1H-NMR and mass spectral data. The newly synthesized compounds are evaluated for their antibacterial activities. Compounds containing nitrofuran moiety showed excellent antibacterial activity. Results of such studies are disscussed in this paper.
