Category: 33342-65-3

In an article, published in an article, once mentioned the application of 33342-65-3, Name is 2-Chloro-5-methylthiazole,molecular formula is C4H4ClNS, is a conventional compound. this article was the specific content is as follows.Formula: C4H4ClNS

Synthetic approaches towards CGA 293’343 (ISO draft common name: thiamethoxam), a novel broad-spectrum insecticide from the class neonicotinoids, are described. 2-Chloro-5-chloromethylthiazole, an important synthetic intermediate, was prepared from five different precursors. Alternatively, CGA 293’343 was prepared via the intermediate 2-benzylmercapto-5-chloromethylthiazole, the synthesis of which is also described.

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Reference：
Thiazole | C3H3027NS – PubChem,
Thiazole | chemical compound | Britannica

Reference of 33342-65-3, Chemistry can be defined as the study of matter and the changes it undergoes. You¡¯ll sometimes hear it called the central science because it is the connection between physics and all the other sciences, starting with biology.33342-65-3, Name is 2-Chloro-5-methylthiazole, molecular formula is C4H4ClNS. In a patent, introducing its new discovery.

An azo-dye lead was modified to a novel N-(1,3-thiazol-2-yl)pyridin-2-amine series of KDR kinase inhibitors through the use of rapid analog libraries. This new class has been found to be potent, selective, and of low molecular weight. Molecular modeling has postulated an interesting conformational preference and binding mode for these compounds in the active site of the enzyme.

An azo-dye lead was modified to a novel N-(1,3-thiazol-2-yl)pyridin-2-amine series of KDR kinase inhibitors through the use of rapid analog libraries. This new class has been found to be potent, selective, and of low molecular weight. Molecular modeling has postulated an interesting conformational preference and binding mode for these compounds in the active site of the enzyme.

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Reference£º
Thiazole | C3H3032NS – PubChem,
Thiazole | chemical compound | Britannica

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.33342-65-3, Name is 2-Chloro-5-methylthiazole, molecular formula is C4H4ClNS. In a Patent£¬once mentioned of 33342-65-3, Quality Control of: 2-Chloro-5-methylthiazole

The invention relates to of the thiamethoxam key intermediate 2 – chloro – 5 – chloromethyl-thiazole preparation method, to overcome the disadvantages of the prior art, by selection of appropriate reaction raw materials, can be prepared at room temperature intermediate 2 – chloro – 5 – chloromethyl-thiazole, without the need of cooling equipment, energy saving, and can improve the yield of the reaction. (by machine translation)

The invention relates to of the thiamethoxam key intermediate 2 – chloro – 5 – chloromethyl-thiazole preparation method, to overcome the disadvantages of the prior art, by selection of appropriate reaction raw materials, can be prepared at room temperature intermediate 2 – chloro – 5 – chloromethyl-thiazole, without the need of cooling equipment, energy saving, and can improve the yield of the reaction. (by machine translation)

The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 33342-65-3 is helpful to your research., Quality Control of: 2-Chloro-5-methylthiazole

Reference£º
Thiazole | C3H3025NS – PubChem,
Thiazole | chemical compound | Britannica