868662-63-9 Usage
General Description
2-TRIFLUOROMETHYLQUINOLINE-7-CARBOXYLIC ACID, also known as 2-trifluoromethyl-7-quinolinecarboxylic acid, is a chemical compound with the molecular formula C11H6F3NO2. It is a derivative of quinoline and contains a carboxylic acid functional group and a trifluoromethyl group. 2-TRIFLUOROMETHYLQUINOLINE-7-CARBOXYLIC ACID has been studied for its potential use in pharmaceuticals and agrochemicals, as well as for its fluorescent properties in organic electronics. It has also been found to exhibit antiangiogenic and antiproliferative effects, making it a potential candidate for cancer therapy. Additionally, 2-trifluoromethylquinoline-7-carboxylic acid has been investigated for its antimicrobial and antibacterial properties, which could have applications in the development of new antibiotics.
Check Digit Verification of cas no
The CAS Registry Mumber 868662-63-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,8,6,6 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 868662-63:
(8*8)+(7*6)+(6*8)+(5*6)+(4*6)+(3*2)+(2*6)+(1*3)=229
229 % 10 = 9
So 868662-63-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H6F3NO2/c12-11(13,14)9-4-3-6-1-2-7(10(16)17)5-8(6)15-9/h1-5H,(H,16,17)
868662-63-9Relevant articles and documents
New regiospecific synthesis of 2-trifluoromethyl-1,5 diazapentadiene compounds and of 2-trifluoromethylquinolines, their cyclization products
El Kharrat, Salem,Skander, Myriem,Dahmani, Abdelkader,Laurent, Philippe,Blancou, Hubert
, p. 8327 - 8331 (2005)
2-Trifluoromethylquinolines 5 are synthesized in high yields using a perfluoroalkylated gemiodoacetoxy derivative 3 and arylamines 4. The intermediate of this reaction, 2-trifluoromethyl-1,5-diazapentadiene compound 6, was isolated. The procedures are eas
