957062-61-2 Usage
Uses
Used in Pharmaceutical Research:
4-Bromo-1-butyl-1H-pyrazole is used as a building block for the synthesis of various biologically active molecules, contributing to the development of new drugs and other chemical products. Its unique chemical structure allows for the creation of compounds with potential therapeutic effects, making it a valuable asset in the field of pharmaceutical research.
Used in Chemical Product Development:
As an intermediate in the synthesis of new chemical products, 4-Bromo-1-butyl-1H-pyrazole plays a crucial role in the development of innovative materials and compounds. Its versatility and unique properties enable the creation of a wide range of products with diverse applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 957062-61-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,7,0,6 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 957062-61:
(8*9)+(7*5)+(6*7)+(5*0)+(4*6)+(3*2)+(2*6)+(1*1)=192
192 % 10 = 2
So 957062-61-2 is a valid CAS Registry Number.
957062-61-2Relevant academic research and scientific papers
Synthesis and Evaluation of Pyrazole Derivatives as Potent Antinemic Agents
Dhillon, N. K.,Jain, N.,Kaur, G.,Utreja, D.
, p. 113 - 118 (2020/03/25)
Pyrazole derivatives were synthesized by bromination of pyrazole, followed by N-alkylation of 4-bromopyrazole. The synthesized derivatives were characterized by microanalytical data and IR and 1H and 13C NMR spectra and were evaluated for their nematicidal activity against the root knot nematode Meloidogyne incognita. The compounds were screened for their egg hatch inhibition and mortality potential, and they showed significant nematicidal activity as compared to the control. 1H-Pyrazol-5(4H)-one was found to be most effective in egg hatch inhibition, and 4-bromopyrazole was found to be most effective in juvenile mortality.
Direct C-H Alkenylation of Functionalized Pyrazoles
Han, Su Jin,Kim, Hyun Tae,Joo, Jung Min
, p. 689 - 698 (2016/01/27)
We have developed inter- and intramolecular C-H alkenylation reactions of pyrazoles. The catalyst, derived from Pd(OAc)2 and pyridine, enabled the oxidative alkenylation of pyrazoles containing a variety of functional groups at the C4 position.
