299162-83-7 Usage
General Description
1-(4-Fluorophenyl)-5-phenyl-1H-pyrazole is a chemical compound that belongs to the class of pyrazole derivatives. It is classified as an arylpyrazole and contains a fluorine substituted phenyl group and a phenyl group. 1-(4-FLUOROPHENYL)-5-PHENYL-1H-PYRAZOLE has potential applications in medicinal chemistry and pharmaceutical research, as pyrazole derivatives have been found to exhibit a wide range of biological activities, including anti-inflammatory, analgesic, antihypertensive, and antitumor properties. Its unique structure and functional groups make it a potential candidate for further study and development of new drugs with therapeutic benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 299162-83-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,9,1,6 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 299162-83:
(8*2)+(7*9)+(6*9)+(5*1)+(4*6)+(3*2)+(2*8)+(1*3)=187
187 % 10 = 7
So 299162-83-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H11FN2/c16-13-6-8-14(9-7-13)18-15(10-11-17-18)12-4-2-1-3-5-12/h1-11H
299162-83-7Relevant articles and documents
Copper-mediated tandem ring-opening/cyclization reactions of cyclopropanols with aryldiazonium salts: Synthesis of: N -arylpyrazoles
Liu, Jidan,Xu, Erjie,Jiang, Jinyuan,Huang, Zeng,Zheng, Liyao,Liu, Zhao-Qing
supporting information, p. 2202 - 2205 (2020/02/26)
A general method for the synthesis of structurally diverse N-arylpyrazoles from readily available cyclopropanols and aryldiazonium salts is disclosed. The reaction was conducted at room temperature within minutes with a broad substrate scope and excellent regioselectivity.