72411-49-5 Usage
Uses
Used in Pharmaceutical Industry:
1-(4-Chlorophenyl)-3-phenyl-1H-pyrazol-5-ylamine is used as a pharmaceutical compound for its potential therapeutic applications in treating inflammatory and cancer-related conditions. Its anti-inflammatory, analgesic, and anticancer properties make it a promising candidate for the development of new drugs to address these health issues.
Used in Drug Development:
In the field of drug development, 1-(4-Chlorophenyl)-3-phenyl-1H-pyrazol-5-ylamine is utilized as a key building block for creating new drug candidates. Its ability to act as a ligand for various biological targets allows researchers to explore its potential in designing novel medications with improved efficacy and selectivity.
Used in Research Settings:
1-(4-Chlorophenyl)-3-phenyl-1H-pyrazol-5-ylamine is also used as a research compound in various scientific studies. Its pharmacological activities and potential as a ligand make it an important tool for investigating the underlying mechanisms of diseases and for identifying new therapeutic targets.
Check Digit Verification of cas no
The CAS Registry Mumber 72411-49-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,4,1 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 72411-49:
(7*7)+(6*2)+(5*4)+(4*1)+(3*1)+(2*4)+(1*9)=105
105 % 10 = 5
So 72411-49-5 is a valid CAS Registry Number.
72411-49-5Relevant academic research and scientific papers
VILSMEIER-HAACK REACTION OF 5-AMINO- AND 5-ACYLAMINO-PYRAZOLES
Simay, A.,Takacs, K.,Horvath, K.,Dvortsak, P.
, p. 127 - 140 (2007/10/02)
The Vilsmeier-Haack reaction of 5-aminopyrazole derivatives 1 was investigated in view of contradictory literature reports.Structure 2 of the products was proved both chemically and spectroscopically.The mechanism of the reaction was postulated on the basis of isolated intermediates 7 and 8. 5-Acylaminopyrazoles 9, 10 and 11 were found to give also 2 (and 7) under the Vilsmeier conditions by an acyl splitting reaction, proceeding probably via diacylamino derivatives 12.Compounds 2 provided a simple route to pyrazolopyrimidine derivatives 13 and 14 as well as to azomethine compounds 15-18.
