Simple exploration of 682342-65-0

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Children learn through play, and they learn more than adults might expect. Science experiments are a great way to spark their curiosity, get their minds active, and encourage them to do something that doesn’t involve a screen. 682342-65-0, C4H2F3IN2S. A document type is Patent, introducing its new discovery., Product Details of 682342-65-0

Insecticidal aminothiazole derivatives and the use as an insecticide and acaricide of the compounds of formula (1): 1wherein R1 is cyano or fluoroalkyl, R2 is halogen, SCN or aryl, R3 is H, C1-C6 alkyl, SO2R5 or C(O)R6, R4 and R6 are, independently, aryl, phenylalkyl, alkyl, cycloalkyl groups, being optionally substituted by one or more of halogen, cyano, alkyl, alkenyl, alkynyl, haloalkyl, alkoxy, nitro, alkoxycarbonyl, alkylcarbonyloxy, alkylenedioxy, alkylcarbonyl, amino, alkylamino, haloalkoxy, alkylthio, alkylsulfonyl, haloalkenyl, alkoxycarbonylalkyl or alkoxycarbonylalkoxy; said aryl, phenylalkyl groups may additionally be fused to a cycloalkyl ring, R5 is C1-C6 alkyl, haloalkyl, X is O, S, NR7, R7 is alkyl, cycloalkyl, alkoxy, alkenylalkyloxy, alkynylalkyloxy, alkoxycarbonylalkyloxy.

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Reference:
Thiazole | C3H6415NS – PubChem,
Thiazole | chemical compound | Britannica

Simple exploration of 682342-65-0

682342-65-0 5-Iodo-4-(trifluoromethyl)thiazol-2-amine 22717671, athiazole compound, is more and more widely used in various.

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.682342-65-0,5-Iodo-4-(trifluoromethyl)thiazol-2-amine,as a common compound, the synthetic route is as follows.,682342-65-0

2-Amino-5-iodo-4-trifluoromethylthiazole (1.2 g) was dissolved in pyridine (2 ml) and thiophene-2-carbonyl chloride (0.80 g) was added at room temperature with stirring. The mixture was stirred for 6 hr at room temperature. The mixture was poured into ice water and acidified with aqueous hydrochloric acid then extracted with chloroform. The chloroform layer was dried over magnesium sulfate and the solvent was removed under reduced pressure. The solid thus obtained was recrystallized from methanol to give N-(5-iodo-4-trifluoromethylthiazol-2-yl)thiophene-2-carboxamide (1.2 g), m. p. 184-185 C.

682342-65-0 5-Iodo-4-(trifluoromethyl)thiazol-2-amine 22717671, athiazole compound, is more and more widely used in various.

Reference£º
Patent; Nippon Soda Co., Ltd.; US2004/82629; (2004); A1;,
Thiazole | C3H3NS – PubChem
Thiazole | chemical compound | Britannica