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3-([1,1'-biphenyl]-4-yl)-5-phenyl-1H-pyrazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51813-17-3

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51813-17-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51813-17-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,8,1 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 51813-17:
(7*5)+(6*1)+(5*8)+(4*1)+(3*3)+(2*1)+(1*7)=103
103 % 10 = 3
So 51813-17-3 is a valid CAS Registry Number.

51813-17-3Downstream Products

51813-17-3Relevant academic research and scientific papers

Copper-Promoted Oxidative Intramolecular C–H Amination of Hydrazones to Synthesize 1H-Indazoles and 1H-Pyrazoles Using a Cleavable Directing Group

Zhang, Guofu,Fan, Qiankun,Zhao, Yiyong,Ding, Chengrong

, p. 5801 - 5806 (2019/08/02)

A facile and efficient synthesis of 1H-indazoles and 1H-pyrazoles through a copper-promoted oxidative intramolecular C–H amination of hydrazones using a cleavable directing group was developed. This reaction is characterized by its mild conditions, operational simplicity, readily available reagents, and excellent yields. A tentative mechanism for Cu-mediated C–H oxidative amination was proposed.

Preparation and structures of some new 1H-pyrazole derivatives

Wang, Dun-Jia,Kang, Yan-Fang,Zheng, Chun-Yang,Wei, Xian-Hong

, p. 2311 - 2320 (2013/07/26)

Some new 3,5-diaryl-1H-pyrazoles were prepared from aryl methyl ketones via Claisen condensation with aromatic esters and followed by cyclization with hydrazine monohydrate. Their structures were confirmed by IR, 1H NMR spectroscopy, mass spect

Solvent free synthesis of different substituted pyrazoles under microwave irradiation via one pot synthesis and their biological evaluation

Shorey, Shweta,Choudhary, Prakash,Intodia, Kumud

, p. 5930 - 5932,3 (2020/09/15)

Pyrazoles and their derivative are widely used as pharmaceutical and agrochemical agents and consequently a large number of synthetic routes to pyrazole have been reported. Due to the property of reducing blood sugar by pyrazole, it has resulted in the sy

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