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Phenol, 2-(1,3-diphenyl-1H-pyrazol-5-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19726-11-5

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19726-11-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19726-11-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,2 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19726-11:
(7*1)+(6*9)+(5*7)+(4*2)+(3*6)+(2*1)+(1*1)=125
125 % 10 = 5
So 19726-11-5 is a valid CAS Registry Number.

19726-11-5Downstream Products

19726-11-5Relevant academic research and scientific papers

Diversity-oriented synthesis of pyrazoles derivatives from flavones and isoflavones leads to the discovery of promising reversal agents of fluconazole resistance in Candida albicans

Cui, Chang-Yi,Liu, Jun,Zheng, Hong-Bo,Jin, Xue-Yang,Zhao, Xiao-Yu,Chang, Wen-Qiang,Sun, Bin,Lou, Hong-Xiang

supporting information, p. 1545 - 1549 (2018/04/02)

Diversity-oriented synthesis of derivatives of natural products is an important approach for the discovery of novel drugs. In this paper, a series of novel 3,4-diaryl-1H-pyrazoles and 3,5-diaryl-1H-pyrazoles derivatives were synthesized through the one-po

SYNTHESIS OF SOME ISOMERIC PYRAZOLES

Sharma, T. C.,Pawar, S. R.,Reddy, N. J.

, p. 159 - 162 (2007/10/02)

The syntheses of 3-o-hydroxyphenyl-1,5-diphenylpyrazoles (III) and 1,3-diphenyl-5-o-hydroxyphenylpyrazoles (V) by the oxidation of corresponding pyrazolines (II) with manganese dioxide and by the reaction of phenylhydrazine with 2'-hydroxychalcone dibromi

The Preparation of 5-Phenacylisoxazoles and 5-Hydroxyphenylisoxazoles and -pyrazoles by the Condensation of C(α)-Dianions with Ethyl Benzoylacetate and Methyl Salicylate

Livingston, Melanie J.,Chick, MarLisa F.,Shealy, Ernest O.,Beam, Charles F.

, p. 215 - 217 (2007/10/02)

C(α),O-Dilithiooximes and C(α),N-Dilithiophenylhydrazones were prepared in an excess of lithium diisopropylamide (LDA).The former was condensed with ethyl benzoylacetate and methyl salicylate, and the latter condensed with methyl salicylate.The resulting precyclization intermediates were than treated with aqueous acid, which was followed by cyclodehydration to give phenacylisoxazoles and hydroxyphenylisoxazoles and -pyrazoles.

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