299162-81-5 Usage
Description
1-(4-bromophenyl)-5-phenyl-1H-pyrazole is a pyrazole derivative, a heterocyclic organic compound characterized by a five-membered ring with two nitrogen atoms. This specific compound features a molecular formula of C15H11BrN2 and is distinguished by the presence of a bromine atom attached to a phenyl ring at the first position and another phenyl group at the fifth position of the pyrazole ring. Its structural properties suggest potential applications in pharmaceutical research and the possibility of exhibiting biological activity.
Uses
Used in Pharmaceutical Research:
1-(4-bromophenyl)-5-phenyl-1H-pyrazole is used as a chemical compound in pharmaceutical research for its potential to exhibit biological activity. Its unique structure with a bromine atom and phenyl groups may contribute to its interaction with biological targets, making it a promising candidate for the development of new drugs.
Used in Organic Synthesis:
In the field of organic chemistry, 1-(4-bromophenyl)-5-phenyl-1H-pyrazole is used as a building block for the synthesis of other organic compounds. Its structural features allow for further chemical modifications and reactions, facilitating the creation of a diverse range of molecules with various applications in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 299162-81-5 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 299162-81:
(8*2)+(7*9)+(6*9)+(5*1)+(4*6)+(3*2)+(2*8)+(1*1)=185
185 % 10 = 5
So 299162-81-5 is a valid CAS Registry Number.
299162-81-5Relevant 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
, 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.
