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4-methyl-1,3-diphenyl-1H-pyrazole is a chemical compound with the molecular formula C17H15N2. It is a derivative of pyrazole, a five-membered heterocyclic ring containing three carbon atoms and two nitrogen atoms. The compound features a methyl group (-CH3) at the 4-position, and two phenyl groups (C6H5) attached to the 1 and 3 positions of the pyrazole ring. This organic molecule is known for its potential applications in various fields, such as pharmaceuticals and materials science, due to its unique structure and properties. It can be synthesized through various chemical reactions and is often used as a building block for more complex molecules.

7188-93-4

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7188-93-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7188-93-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,8 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7188-93:
(6*7)+(5*1)+(4*8)+(3*8)+(2*9)+(1*3)=124
124 % 10 = 4
So 7188-93-4 is a valid CAS Registry Number.

7188-93-4Downstream Products

7188-93-4Relevant academic research and scientific papers

Practical synthesis of pyrazoles via a copper-catalyzed relay oxidation strategy

Tang, Xiaodong,Huang, Liangbin,Yang, Jidan,Xu, Yanli,Wu, Wanqing,Jiang, Huanfeng

supporting information, p. 14793 - 14796 (2014/12/11)

Various 1,3- and 1,3,4-substituted pyrazoles are smoothly formed via copper-catalyzed cascade reactions of oxime acetates, amines and aldehydes. This relay oxidative process involves copper-promoted N-O bond cleavage and C-C/C-N/N-N bond formations to furnish pyrazolines, and sequential Cu-O2 system-involved oxidative dehydrogenation of pyrazolines to afford pyrazoles. This transformation provides a novel and versatile approach for the synthesis of pyrazoles, with an inexpensive copper catalyst and green oxidants. It is atom- and step-economical, and possesses a good functional group tolerance, as well as operational simplicity. This journal is

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