157848-08-3 Usage
Description
5,7-DICHLORO-4-HYDROXY-QUINOLINE-2-CARBOXYLIC ACID ETHYL ESTER is a quinoline derivative that serves as an ethyl ester derivative of 5,7-dichloro-4-hydroxyquinoline-2-carboxylic acid. It is recognized for its potential antimicrobial, antiviral, and anticancer properties, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals.
Uses
Used in Pharmaceutical Industry:
5,7-DICHLORO-4-HYDROXY-QUINOLINE-2-CARBOXYLIC ACID ETHYL ESTER is used as an intermediate in the synthesis of various pharmaceuticals for its potential antimicrobial, antiviral, and anticancer properties. It plays a crucial role in the development of new therapeutic agents to combat infectious diseases and cancer.
Used in Agrochemical Industry:
In the agrochemical sector, 5,7-DICHLORO-4-HYDROXY-QUINOLINE-2-CARBOXYLIC ACID ETHYL ESTER is utilized as an intermediate in the production of agrochemicals, leveraging its antimicrobial properties to protect crops from diseases and pests, thereby enhancing agricultural productivity.
Safety Considerations:
It is essential to handle 5,7-DICHLORO-4-HYDROXY-QUINOLINE-2-CARBOXYLIC ACID ETHYL ESTER with proper care and adhere to safety protocols to minimize health hazards. This chemical may pose risks if not used and stored correctly, emphasizing the need for cautious handling in both research and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 157848-08-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,8,4 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 157848-08:
(8*1)+(7*5)+(6*7)+(5*8)+(4*4)+(3*8)+(2*0)+(1*8)=173
173 % 10 = 3
So 157848-08-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H9Cl2NO3/c1-2-18-12(17)9-5-10(16)11-7(14)3-6(13)4-8(11)15-9/h3-5H,2H2,1H3,(H,15,16)
157848-08-3Relevant articles and documents
Process for preparing 1,4-dihydro-4-oxoquinoline-2-carboxylates and 4-aminoquinoline compounds therefrom
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Page/Page column 18-20, (2021/01/17)
A method for preparing an alkyl 5,7-dihalo-1,4-dihydro-4-oxoquinoline-2-carboxylate ester is described herein. The method comprises cyclizing a compound of Formula III with Eaton's reagent in heated continuous flow reactor to form a compound of Formula IV
Heterocyclic benzenesulfonylimine derivatives as inhibitors of IL-1 action
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, (2008/06/13)
The present invention relates to heterocyclic benzenesulfonylimine derivatives and their use as inhibitors of Interleukin-1 (IL-1) action. Such inhibitors are useful in the treatment of various disease states as disclosed herein including rheumatoid arthr
