Discover the magic of the 3,5-Dimethyl-1H-pyrazole

Product Details of 67-51-6. Bye, fridends, I hope you can learn more about C5H8N2, If you have any questions, you can browse other blog as well. See you lster.

An article Oxidation of sulfides in aqueous media catalyzed by pyrazole-oxidoperoxido-molybdenum(VI) complexes WOS:000552643400003 published article about MOLYBDENUM(VI) COMPLEXES; MOLECULAR-STRUCTURE; METAL DERIVATIVES; OXYGEN-TRANSFER; SULFOXIDES; CHEMISTRY; PYRAZOLE; CRYSTAL; POLY(PYRAZOLYL)ALKANES; COORDINATION in [Bruno, Sofia M.; Amarante, Tatiana R.; Paz, Filipe A. Almeida; Pillinger, Martyn; Valente, Anabela A.; Goncalves, Isabel S.] Univ Aveiro, Dept Chem, CICECO Aveiro Inst Mat, Campus Univ Santiago, P-3810193 Aveiro, Portugal in 2020.0, Cited 39.0. Product Details of 67-51-6. The Name is 3,5-Dimethyl-1H-pyrazole. Through research, I have a further understanding and discovery of 67-51-6

The complex [MoO(O-2)(2)(pyrazole)(2)] (1) is an effective catalyst for the oxidation of organic sulfides (methyl-phenylsulfide and diphenylsulfide). Reactions can be run in water as the only medium, at low temperature (25 degrees C), with low catalyst loadings (0.2 mol%) and excellent H2O2 efficiency with no significant non-productive decomposition of the oxidant. Under conditions that favor sulfone formation, the overall process, including isolation of the precipitated product (by filtration or centrifugation) and recycling of the aqueous phase con-taining the catalyst, can be performed in the absence of organic or ionic liquid solvents. Catalytic results with the recycled aqueous phase were the same as those obtained in the first cycle. With water as the sole solvent, 1 is a superior catalyst to the 3,5-dimethylpyrazole complexes [MoO(O-2)(2)(dmpz)(2)] (2) and [Hdmpz](4)[Mo8O25.8(O-2)(0.2)(dmpz)(2)]center dot 4H(2)O (3). Crystal structures for 1 and 3 are presented.

Product Details of 67-51-6. Bye, fridends, I hope you can learn more about C5H8N2, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics