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3-chloro-5-isoxazolecarboxylic acid (SALTDATA: FREE) is an isoxazolecarboxylic acid derivative featuring a chlorine atom at the 3-position of the isoxazole ring. This chemical compound is recognized for its wide-ranging applications in the pharmaceutical industry, where it serves as a key building block for the synthesis of diverse bioactive molecules. Its antimicrobial and herbicidal properties further extend its utility in the production of agrochemicals and pigments, making it a highly sought-after and significant entity in the realm of organic chemistry.

20724-56-5

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20724-56-5 Usage

Uses

Used in Pharmaceutical Industry:
3-chloro-5-isoxazolecarboxylic acid (SALTDATA: FREE) is used as a building block for the synthesis of various bioactive molecules, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Production:
3-chloro-5-isoxazolecarboxylic acid (SALTDATA: FREE) is utilized as an ingredient in the production of agrochemicals, capitalizing on its antimicrobial and herbicidal properties to enhance crop protection and yield.
Used in Pigment Industry:
This chemical compound is employed in the manufacturing of pigments, leveraging its chemical properties to contribute to the coloration and stability of various products.
Used in Antimicrobial Applications:
3-chloro-5-isoxazolecarboxylic acid (SALTDATA: FREE) is used as an antimicrobial agent for its ability to inhibit the growth of microorganisms, finding applications in various industries where microbial control is essential.
Used in Herbicidal Applications:
Leveraging its herbicidal properties, 3-chloro-5-isoxazolecarboxylic acid (SALTDATA: FREE) is used in the development of herbicides to control unwanted plant growth in agricultural and horticultural settings.

Check Digit Verification of cas no

The CAS Registry Mumber 20724-56-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,7,2 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 20724-56:
(7*2)+(6*0)+(5*7)+(4*2)+(3*4)+(2*5)+(1*6)=85
85 % 10 = 5
So 20724-56-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H2ClNO3/c5-3-1-2(4(7)8)9-6-3/h1H,(H,7,8)

20724-56-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-1,2-oxazole-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-chloro-5-isoxazolecarboxylic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:20724-56-5 SDS

20724-56-5Relevant academic research and scientific papers

SUBSTITUTED BENZIMDAZOLE DERIVATIVES USEFUL AS TRPM8 RECEPTOR MODULATORS

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Page/Page column 43, (2012/08/27)

The present invention is directed to benzimidazole derivatives, pharmaceutical compositions containing them and their use in the treatment of disorders and conditions modulated by TRP M8, including for example, inflammatory pain, inflammatory hyperalgesia

SYNTHESIS OF 3-HALOISOXAZOLES BY NOVEL OXIDATIVE DEGRADATION OF THE SIDE-CHAIN OF 3-(3-HALO-ISOXAZOL-5-YL) PROPIONIC ACIDS

Lugosi, Peter,Schawartz, Jozsef,Doleschall, Gabor

, p. 3061 - 3066 (2007/10/02)

A novel method for the oxidative degradation of the side-chain of 3-(3-haloisoxazol-5-yl) propionic acids has been developed.The E-3-(3-chloroisoxazol-5-yl) propenoic acid 13a obtained by treatment of the s-triazolo quinazolin-4-ium iodide 11a with PhI(OAc)2 and Bz2O2, respectively, and subsequent hydroxysis, has been used for the synthesis of numerous 3-haloisoxazole derivatives.

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