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1H-Pyrazole, 1-(4-bromophenyl)-3-methyl-5-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90276-21-4

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90276-21-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90276-21-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,7 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 90276-21:
(7*9)+(6*0)+(5*2)+(4*7)+(3*6)+(2*2)+(1*1)=124
124 % 10 = 4
So 90276-21-4 is a valid CAS Registry Number.

90276-21-4Downstream Products

90276-21-4Relevant academic research and scientific papers

TBHP/Cu(OAc)2 mediated oxidation of pyrazolines: A convenient method for the preparation of pyrazoles

Kolla, Sai Teja,Somanaboina, Ramya,Bhimapaka, China Raju

, p. 1425 - 1432 (2021/02/27)

An efficient and simple oxidative protocol has been developed for the preparation of pyrazoles from pyrazolines mediated by TBHP/Cu(OAc)2 at room temperature. The present protocol has been successfully applied for the preparation of various pyrazole compounds from heterocyclic pyrazolines.

Copper-catalyzed aerobic C(sp2)-H functionalization for C-N bond formation: Synthesis of pyrazoles and indazoles

Li, Xianwei,He, Li,Chen, Huoji,Wu, Wanqing,Jiang, Huanfeng

, p. 3636 - 3646 (2013/06/04)

A simple, practical, and highly efficient synthesis of pyrazoles and indazoles via copper-catalyzed direct aerobic oxidative C(sp2)-H amination has been reported herein. This process tolerated a variety of functional groups under mild conditions. Further diversification of pyrazoles was also investigated, which provided its potential for drug discovery.

Highly regioselective synthesis of 1-aryl-3,4,5-substituted pyrazoles

Gosselin, Francis,O'Shea, Paul D.,Webster, Robert A.,Reamer, Robert A.,Tillyer, Richard D.,Grabowski, Edward J. J.

, p. 3267 - 3270 (2008/09/17)

A highly regioselective synthesis of 1-aryl-3,4,5-substituted pyrazoles based on the condensation of 1,3-diketones with arylhydrazines is described. The reaction proceeds at room temperature in N,N-dimethylacetamide and furnishes pyrazoles in 59-98% yield

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