118791-14-3 Usage
Uses
Used in Pharmaceutical Industry:
6-Chloroquinoline-3-carboxylic acid is used as a key intermediate in the synthesis of antimalarial drugs. Its unique chemical structure contributes to the development of effective treatments against malaria, a disease affecting millions of people worldwide.
Used in Agrochemical Industry:
In the agrochemical sector, 6-Chloroquinoline-3-carboxylic acid is utilized as a precursor for the production of insecticides. Its incorporation into these products helps control and eliminate pests, thereby protecting crops and ensuring food security.
Used in Organic Synthesis:
6-Chloroquinoline-3-carboxylic acid is employed as an intermediate in the manufacturing of various organic compounds. Its versatile chemical properties allow it to be a valuable building block for the synthesis of a wide range of molecules with diverse applications.
It is important to handle 6-Chloroquinoline-3-carboxylic acid with care due to its potential health hazards and environmental impact. Proper safety measures should be taken during its production, use, and disposal to minimize any adverse effects.
Check Digit Verification of cas no
The CAS Registry Mumber 118791-14-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,7,9 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 118791-14:
(8*1)+(7*1)+(6*8)+(5*7)+(4*9)+(3*1)+(2*1)+(1*4)=143
143 % 10 = 3
So 118791-14-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H6ClNO2/c11-8-1-2-9-6(4-8)3-7(5-12-9)10(13)14/h1-5H,(H,13,14)
118791-14-3Relevant articles and documents
Chemical compounds
-
, (2008/06/13)
Provided herein are novel and useful compounds having a tryptase inhibition activity, pharmaceutical compositions comprising such compounds, and methods treating subjects suffering from a condition, disease, or disorder that can be ameliorated by the administration of an inhibitor of tryptase, e.g., asthma and inflammatory diseases, to name only a few.
Syntheses and Reactions of Diazepinoquinolines
Guendel, Wolf-H.,Bohnert, Sabine
, p. 769 - 777 (2007/10/02)
Three routes for the preparation of diazepinoquinolines (1) have been studied.The best yields resulted by starting from the amides of N-(3-quinolylcarbonyl)-N-alkyl-amino acids (5).Quaternization to 9, intramolecular cyclization under the influence of base to 10, oxidation to 11 and debenzylation by catalytic hydrogenation gave 1. - Keywords: Quinolinium Salts, Cyclization Reaction
