24567-08-6 Usage
Description
3,4-diphenyl-2H-pyrazole, also known as diphenylpyrazole, is a heterocyclic organic compound with the molecular formula C16H14N2. It features a pyrazole ring with two phenyl groups attached at positions 3 and 4, offering a versatile structure for various applications in different industries.
Uses
Used in Pharmaceutical and Agrochemical Industries:
3,4-diphenyl-2H-pyrazole is used as a building block for the synthesis of various pharmaceutical drugs and agrochemicals. Its unique structure allows for the development of new compounds with potential therapeutic and pesticidal properties.
Used in Coordination Chemistry:
3,4-diphenyl-2H-pyrazole is used as a ligand in coordination chemistry. Its ability to form stable complexes with metal ions makes it a valuable component in the design of new materials with specific catalytic, electronic, or optical properties.
Used in Optoelectronic Devices:
3,4-diphenyl-2H-pyrazole is used as a component in organic light-emitting diodes (OLEDs) and other optoelectronic devices. Its electronic properties contribute to the performance and efficiency of these devices.
Used in Antimicrobial and Anti-inflammatory Applications:
3,4-diphenyl-2H-pyrazole has been studied for its potential biological activities, including antimicrobial and anti-inflammatory properties. Its ability to inhibit microbial growth and reduce inflammation may lead to the development of new treatments for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 24567-08-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,6 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24567-08:
(7*2)+(6*4)+(5*5)+(4*6)+(3*7)+(2*0)+(1*8)=116
116 % 10 = 6
So 24567-08-6 is a valid CAS Registry Number.
InChI:InChI=1/C15H12N2/c1-3-7-12(8-4-1)14-11-16-17-15(14)13-9-5-2-6-10-13/h1-11H,(H,16,17)
24567-08-6Relevant articles and documents
Calcium carbide as the acetylide source: Transition-metal-free synthesis of substituted pyrazoles via [1,5]-sigmatropic rearrangements
Yu, Yue,Huang, Wei,Chen, Yang,Gao, Bingjie,Wu, Wanqing,Jiang, Huanfeng
supporting information, p. 6445 - 6449 (2018/06/08)
Under transition-metal-free conditions, calcium carbide was used as the acetylide source to react with a wide range of N-tosylhydrazones derived from aldehydes or ketones, affording various substituted pyrazoles in good yields with high regioselectivities. The transformations go through [3 + 2] cycloadditions followed by [1,5]-sigmatropic rearrangements, which are supported by deuterium-labeling experiments.
Microwave-assisted synthesis of pyrazoles by 1,3-dipolar cycloaddition of diazo compounds to acetylene derivatives
Zrinski, Irena,Juribasic, Marina,Eckert-Maksic, Mirjana
, p. 1961 - 1967 (2007/10/03)
Microwave-assisted preparation of a wide range of 5-ethoxycarbonylpyrazoles and 3-pyrazoles by 1,3-dipolar cycloaddition of diazo compound to acetylenes is described. All reactions were carried out using high throughput sequential technique.{A figure is p