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5-(4-fluorophenyl)-1-phenyl-1H-pyrazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

439289-13-1

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439289-13-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 439289-13-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,9,2,8 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 439289-13:
(8*4)+(7*3)+(6*9)+(5*2)+(4*8)+(3*9)+(2*1)+(1*3)=181
181 % 10 = 1
So 439289-13-1 is a valid CAS Registry Number.

439289-13-1Downstream Products

439289-13-1Relevant academic research and scientific papers

Novel crown ether functionalized imidazolium-based acidic ionic liquid catalyzed synthesis of pyrazole derivatives under solvent-free conditions

Patil, Dayanand,Chandam, Dattatraya,Mulik, Abhijeet,Jagdale, Suryabala,Patil, Prasad,Deshmukh, Madhukar

, p. 6843 - 6858 (2015)

Abstract An innovatively designed novel crown ether functionalized imidazolium-based reusable acidic ionic liquid [crown ether MIm] [HSO4] has been efficiently implemented for the synthesis of pyrazole derivatives using various substituted enaminones, hydrazine hydrate and phenyl hydrazine under solvent-free conditions. Structural novelty and task efficiency of the catalyst, high yields of desired products, greener approach attributing high atom economy and solvent-free conditions render this protocol suitable to cope with the current demand in contemporary organic chemistry. The inventive idea of utilizing crown ether functionalized ionic liquid as a catalyst was for the first time demonstrated in this protocol.

Oxone-mediated facile access to substituted pyrazoles

Kashiwa, Mitsuhiro,Kuwata, Yoshiyuki,Sonoda, Motohiro,Tanimori, Shinji

, p. 304 - 311 (2015/12/30)

An Oxone-mediated transition-metal-free oxidative C-N bond formation has been achieved for the regioselective synthesis of substituted pyrazoles. The reactions accompany the chelation-controlled ortho-oxidation of N-substituted aromatic ring to provide ph

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