75304-67-5 Usage
Uses
Used in Pharmaceutical Industry:
4-[(E)-(4-chlorophenyl)diazenyl]-3,5-dimethyl-1H-pyrazol-1-yl(pyridin-4-yl)methanone is used as a potential drug candidate for [application reason] due to its complex molecular structure and the presence of biologically active groups such as the chlorophenyl and pyridin-4-yl moieties.
Used in Agricultural Industry:
In the agricultural sector, 4-[(E)-(4-chlorophenyl)diazenyl]-3,5-dimethyl-1H-pyrazol-1-yl(pyridin-4-yl)methanone is used as a potential pesticide for [application reason] because of its structural complexity and the possibility of having biological activity that could target pests or weeds.
Used in Research and Development:
4-[(E)-(4-chlorophenyl)diazenyl]-3,5-dimethyl-1H-pyrazol-1-yl(pyridin-4-yl)methanone is also used as a subject of interest for further research and development in [application reason] due to its unique properties and potential for discovering new applications or understanding its biological effects.
Check Digit Verification of cas no
The CAS Registry Mumber 75304-67-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,3,0 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 75304-67:
(7*7)+(6*5)+(5*3)+(4*0)+(3*4)+(2*6)+(1*7)=125
125 % 10 = 5
So 75304-67-5 is a valid CAS Registry Number.
75304-67-5Relevant academic research and scientific papers
Development of Pyrazole Derivatives as Xanthine Oxidase Inhibitors
Akhtar, Md Sayeed,Alsayari, Abdulrhman,Asiri, Yahya I.,Hassan, Mohd. Zaheen,Kamal, Mehnaz,Muhsinah, Abdullatif Bin
, p. 635 - 640 (2022/01/26)
A series of arylhydrazono pyrazoles and aryldiazenyl pyrazoles were prepared by rapid one-pot microwave assisted synthesis. In this method, the synthesis of these pyrazoles was carried out by reacting ethyl acetoacetate/acetylacetone, isoniazid, and aryldiazonium salts under solvent free conditions. All the synthesized compounds were fully characterized by infrared, nuclear magnetic resonance, and mass spectrometry. In vitro xanthine oxidase (XO) inhibitory studies revealed that the presence of bromo group at the phenyl ring had significant XO inhibitory activity.
