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METHYL 2-(4-CHLOROPHENYL)-4-METHYL-1,3-THIAZOLE-5-CARBOXYLATE is a chemical compound that belongs to the class of thiazole carboxylates. It features a methyl group attached to a thiazole ring, with a carboxylate group at the 5-position and a 4-chlorophenyl group at the 2-position. This unique structure endows it with potential applications across various fields, including pharmaceuticals, agrochemicals, and material science.

337924-65-9

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337924-65-9 Usage

Uses

Used in Pharmaceutical Industry:
METHYL 2-(4-CHLOROPHENYL)-4-METHYL-1,3-THIAZOLE-5-CARBOXYLATE is used as a building block for the synthesis of biologically active compounds. Its unique structure allows it to be a valuable component in the development of new drugs, potentially contributing to the treatment of various diseases and conditions.
Used in Agrochemical Industry:
In the agrochemical field, METHYL 2-(4-CHLOROPHENYL)-4-METHYL-1,3-THIAZOLE-5-CARBOXYLATE is used as a precursor in the development of new agrochemical agents. Its properties may contribute to the creation of innovative products that enhance crop protection and yield.
Used in Material Science:
METHYL 2-(4-CHLOROPHENYL)-4-METHYL-1,3-THIAZOLE-5-CARBOXYLATE is utilized in the development of new materials with specific properties and functions. Its unique chemical structure may lead to the creation of materials with tailored characteristics for use in various applications, such as sensors, catalysts, or advanced materials for specific industries.

Check Digit Verification of cas no

The CAS Registry Mumber 337924-65-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,7,9,2 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 337924-65:
(8*3)+(7*3)+(6*7)+(5*9)+(4*2)+(3*4)+(2*6)+(1*5)=169
169 % 10 = 9
So 337924-65-9 is a valid CAS Registry Number.

337924-65-9Relevant academic research and scientific papers

Design, synthesis, and biological evaluation of antiviral agents targeting flavivirus envelope proteins

Li, Ze,Khaliq, Mansoora,Zhou, Zhigang,Post, Carol Beth,Kuhn, Richard J.,Cushman, Mark

experimental part, p. 4660 - 4671 (2009/07/11)

Flavivirus envelope proteins (E proteins) have been shown to play a pivotal role in virus assembly, morphogenesis, and infection of host cells. Inhibition of flavivirus infection of a host cell by means of a small molecule envelope protein antagonist is an attractive strategy for the development of antiviral agents. Virtual screening of the NCI chemical database using the dengue virus envelope protein structure revealed several hypothetical hit compounds. Bioassay results identified a class of thiazole compounds with antiviral potency in cell-based assays. Modification of these lead compounds led to a series of analogues with improved antiviral activity and decreased cytotoxicity. The most active compounds 11 and 36 were effective in the low micromolar concentration range in a cellular assay system.

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