97892-67-6 Usage
Description
2-CHLORO-7-METHOXY-4-METHYL-QUINOLINE is a quinoline derivative with the molecular formula C11H10ClNO, featuring a chlorine atom at the 2 position, a methoxy group at the 7 position, and a methyl group at the 4 position. This chemical compound is widely used in various industries due to its diverse applications and potential uses.
Uses
Used in Pharmaceutical Industry:
2-CHLORO-7-METHOXY-4-METHYL-QUINOLINE is used as a building block for the synthesis of various medications, contributing to the development of new drugs with potential therapeutic benefits.
Used in Antimalarial Applications:
2-CHLORO-7-METHOXY-4-METHYL-QUINOLINE has been studied for its potential antimalarial properties, making it a candidate for the development of treatments against malaria.
Used in Antibacterial Applications:
2-CHLORO-7-METHOXY-4-METHYL-QUINOLINE has also been investigated for its antibacterial properties, indicating its potential use in the development of antibiotics to combat bacterial infections.
Used in Dye and Pigment Production:
2-CHLORO-7-METHOXY-4-METHYL-QUINOLINE has been employed in the production of dyes and pigments, highlighting its versatility in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 97892-67-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,8,9 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 97892-67:
(7*9)+(6*7)+(5*8)+(4*9)+(3*2)+(2*6)+(1*7)=206
206 % 10 = 6
So 97892-67-6 is a valid CAS Registry Number.
97892-67-6Relevant articles and documents
Development of antitubercular compounds based on a 4-quinolylhydrazone scaffold. Further structure-activity relationship studies
Gemma, Sandra,Savini, Luisa,Altarelli, Maria,Tripaldi, Pierangela,Chiasserini, Luisa,Coccone, Salvatore Sanna,Kumar, Vinod,Camodeca, Caterina,Campiani, Giuseppe,Novellino, Ettore,Clarizio, Sandra,Delogu, Giovanni,Butini, Stefania
scheme or table, p. 6063 - 6072 (2009/12/09)
A series of 4-quinolylhydrazones was synthesized and tested in vitro against Mycobacterium tuberculosis. At a concentration of 6.25 μg/mL, most of the newly synthesized compounds displayed 100% inhibitory activity against M. tuberculosis in cellular assays. Further screening allowed the identification of very potent antitubercular agents. Compound 4c was also tested in a time-course experiment and against mtb clinical isolates, displaying interesting results.
