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2-Chloro-4-methyl-5-thiazolecarboxylic acid is a chemical compound characterized by the molecular formula C6H4ClNO2S. It is a versatile intermediate in the synthesis of pharmaceuticals and agrochemicals, known for its antifungal and antibacterial properties. The unique molecular structure of 2-Chloro-4-methyl-5-thiazolecarboxylic acid, featuring a thiazole ring, endows it with a range of biological activities, making it an essential building block in the production of various pharmaceutical and agricultural products and a valuable component in research and development.

40003-48-3

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40003-48-3 Usage

Uses

Used in Pharmaceutical Industry:
2-Chloro-4-methyl-5-thiazolecarboxylic acid is used as an intermediate in the synthesis of drugs for its antifungal and antibacterial properties. It contributes to the development of medications that target a variety of infections and diseases, enhancing the therapeutic arsenal against microbial threats.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Chloro-4-methyl-5-thiazolecarboxylic acid is utilized as a key component in the formulation of crop protection products. Its antifungal and antibacterial properties are harnessed to create effective agents that protect crops from various pathogens, thereby ensuring agricultural productivity and food security.
Used in Medicinal Research and Development:
2-Chloro-4-methyl-5-thiazolecarboxylic acid is employed as a valuable component in medicinal research and development due to its potential to exhibit a range of biological activities. Its unique thiazole ring structure allows for exploration in various therapeutic areas, contributing to the discovery of novel drugs and treatment modalities.
Used in Agricultural Research and Development:
2-Chloro-4-methyl-5-thiazolecarboxylic acid also plays a significant role in agricultural research and development, where its properties are investigated for potential applications in enhancing crop resistance to diseases and improving overall plant health. Its integration into agrochemical products aids in the advancement of sustainable and effective pest management strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 40003-48-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,0,0 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 40003-48:
(7*4)+(6*0)+(5*0)+(4*0)+(3*3)+(2*4)+(1*8)=53
53 % 10 = 3
So 40003-48-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H4ClNO2S/c1-2-3(4(8)9)10-5(6)7-2/h1H3,(H,8,9)

40003-48-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-4-methylthiazole-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-chloro-4-methyl-1,3-thiazole-5-carboxylic 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:40003-48-3 SDS

40003-48-3Relevant academic research and scientific papers

Process for the preparation of thiazolecarboxylic acid chlorides

-

, (2008/06/13)

Disclosed herein is a process for the preparation of a thiazolecarboxylic acid chloride represented by the following general formula (II): STR1 wherein R1 represents a hydrogen or halogen atom, a lower alkyl group, a lower alkoxy group, or a lower alkyl group substituted by a halogen atom or lower alkoxy group, and R2 represents a hydrogen atom, a lower alkyl group, or a lower alkyl group substituted by a halogen atom or lower alkoxy group, which comprises reacting a thiazolecarboxylic acid represented by the following general formula (I): STR2 wherein R1 and R2 have the same meanings as defined with respect to formula (II), with phosgene or trichloromethyl chloroformate in the presence or absence of a catalyst.

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