1204355-48-5 Usage
Uses
Used in Organic Synthesis:
1-tert-butyl-5-phenyl-1H-pyrazole is used as a building block in organic synthesis for the creation of various complex organic molecules. Its unique structure allows for the formation of diverse chemical entities, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Coordination Chemistry:
As a ligand, 1-tert-butyl-5-phenyl-1H-pyrazole is used in coordination chemistry to form coordination compounds with metal ions. This application is crucial for the development of new materials with specific properties, such as catalysts, sensors, and materials with unique electronic or magnetic characteristics.
Used in Pharmaceutical Research:
1-tert-butyl-5-phenyl-1H-pyrazole is used as a starting material or intermediate in the development of new pharmaceuticals. Its potential biological activities, including anti-inflammatory and anti-tumor effects, make it a promising candidate for the treatment of various diseases and conditions.
Used in Biological Research:
In the field of biological research, 1-tert-butyl-5-phenyl-1H-pyrazole is employed as a tool compound to study its effects on biological systems. This research helps to elucidate the mechanisms of action and potential therapeutic applications of 1-tert-butyl-5-phenyl-1H-pyrazole, contributing to the advancement of medical science.
Check Digit Verification of cas no
The CAS Registry Mumber 1204355-48-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,4,3,5 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1204355-48:
(9*1)+(8*2)+(7*0)+(6*4)+(5*3)+(4*5)+(3*5)+(2*4)+(1*8)=115
115 % 10 = 5
So 1204355-48-5 is a valid CAS Registry Number.
1204355-48-5Relevant academic research and scientific papers
Oxone-mediated facile access to substituted pyrazoles
Kashiwa, Mitsuhiro,Kuwata, Yoshiyuki,Sonoda, Motohiro,Tanimori, Shinji
, p. 304 - 311 (2015/12/30)
An Oxone-mediated transition-metal-free oxidative C-N bond formation has been achieved for the regioselective synthesis of substituted pyrazoles. The reactions accompany the chelation-controlled ortho-oxidation of N-substituted aromatic ring to provide ph
