Category: 72850-52-3

In an article, published in an article, once mentioned the application of 72850-52-3, Name is Ethyl 2-chloro-4-(trifluoromethyl)thiazole-5-carboxylate,molecular formula is C7H5ClF3NO2S, is a conventional compound. this article was the specific content is as follows.Recommanded Product: 72850-52-3

2-(Heteroamino)-4,5-substituted-oxazole/thiazole compounds are antidotes for thiocarbamate, triazine and acetamide herbicides. These antidote compounds are especially effective to safen acetamide herbicides used to control grassy weeds in sorghum.

2-(Heteroamino)-4,5-substituted-oxazole/thiazole compounds are antidotes for thiocarbamate, triazine and acetamide herbicides. These antidote compounds are especially effective to safen acetamide herbicides used to control grassy weeds in sorghum.

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Reference£º
Thiazole | C3H8070NS – PubChem,
Thiazole | chemical compound | Britannica

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 72850-52-3, Name is Ethyl 2-chloro-4-(trifluoromethyl)thiazole-5-carboxylate, molecular formula is C7H5ClF3NO2S. In a Patent£¬once mentioned of 72850-52-3, COA of Formula: C7H5ClF3NO2S

2,4-Disubstituted-5-thiazolecarboxylic acids and derivatives thereof have been found to reduce herbicidal injury of corn, rice and sorghum plants due to the application thereto of acetamide herbicides.

2,4-Disubstituted-5-thiazolecarboxylic acids and derivatives thereof have been found to reduce herbicidal injury of corn, rice and sorghum plants due to the application thereto of acetamide herbicides.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.COA of Formula: C7H5ClF3NO2S. In my other articles, you can also check out more blogs about 72850-52-3

Reference£º
Thiazole | C3H8068NS – PubChem,
Thiazole | chemical compound | Britannica

72850-52-3,With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.72850-52-3,Ethyl 2-chloro-4-(trifluoromethyl)thiazole-5-carboxylate,as a common compound, the synthetic route is as follows.

2-Chloro-4-trifluoromethyl-thiazole-5-carboxylic acid ethyl ester (259 mg, 1.0mmol), sodium ethoxide (23% by weight in ethanol) (0.33 ml, 1.1 mmol) and ethanol (2ml) were heated under reflux for 2 hours. The mixture was partitioned between water andethyl acetate. The organic phase was dried over magnesium sulfate and concentrated togive the product as a yellow gum (187 mg, 70% yield). ^-NMR (400 MHz, CDC13):1.36 (3H, t, Me), 1.45 (3H, t, Me), 4.35 (2H, q, CH2), 4.55 (2H, q, CH2).

As the paragraph descriping shows that 72850-52-3 is playing an increasingly important role.

Reference£º
Patent; SYNGENTA LIMITED; WO2006/24820; (2006); A1;,
Thiazole | C3H3NS – PubChem
Thiazole | chemical compound | Britannica

72850-52-3, Ethyl 2-chloro-4-(trifluoromethyl)thiazole-5-carboxylate is a thiazole compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

72850-52-3, EXAMPLE 49 STR65 Ethyl 2[(diphenylmethyl)amino]-4-(trifluoromethyl)-5thiazolecarboxylate A reaction vessel was charged with 120 ml of toluene and 11.0 g (42.4 mmol) of ethyl 2-chloro-4-trifluoromethyl-5-thiazolecarboxylate (prepared as described in U.S. Pat. No. 4,199,506). Then, 15.5 g (86 mmol) of aminodiphenylmethane was added in one portion. The resulting yellowish-orange solution was refluxed under nitrogen for 9 days. Then, solvent was removed from the mixture under reduced pressure to yield a yellowish-orange solid material, which was flash chromatographed (~38 ml/min) on silica gel using 10% ethyl acetate in hexane solvent. There was obtained 13.2 g of a thick yellow oil which solidified upon standing to a yellow solid product (m.p.=92-95 C.) identified in Table I.

As the paragraph descriping shows that 72850-52-3 is playing an increasingly important role.

Reference£º
Patent; Monsanto Company; US5000775; (1991); A;,
Thiazole | C3H3NS – PubChem
Thiazole | chemical compound | Britannica