56367-26-1 Usage
Uses
Used in Pharmaceutical Research:
5-BUTYL-1(2)H-PYRAZOL-3-YLAMINE is used as a building block for the synthesis of bioactive compounds in pharmaceutical research. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Research:
In agrochemical research, 5-BUTYL-1(2)H-PYRAZOL-3-YLAMINE is utilized as a component in the creation of agrochemicals, contributing to the development of effective and environmentally friendly solutions for agriculture.
Used in Medicinal Chemistry:
5-BUTYL-1(2)H-PYRAZOL-3-YLAMINE is used as a precursor in the field of medicinal chemistry for the development of novel drugs. Its chemical properties enable the design and synthesis of compounds with potential therapeutic benefits.
Used as a Reagent in Organic Synthesis:
5-BUTYL-1(2)H-PYRAZOL-3-YLAMINE is employed as a reagent in organic synthesis for the preparation of other functionalized pyrazole derivatives. Its versatility in chemical reactions allows for the creation of a wide range of pyrazole-based compounds with various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 56367-26-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,6 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56367-26:
(7*5)+(6*6)+(5*3)+(4*6)+(3*7)+(2*2)+(1*6)=141
141 % 10 = 1
So 56367-26-1 is a valid CAS Registry Number.
56367-26-1Relevant academic research and scientific papers
Studies on nonpeptide angiotensin II receptor antagonists. I. Synthesis and biological evaluation of pyrazolo [1,5-b][1,2,4]triazole derivatives with alkyl substituents
Okazaki, Toshio,Suga, Akira,Watanabe, Toshihiro,Kikuchi, Kazumi,Kurihara, Hiroyuki,Shibasaki, Masayuki,Fujimori, Akira,Inagaki, Osamu,Yanagisawa, Isao
, p. 69 - 78 (2007/10/03)
Alkyl-substituted pyrazolo[1,5-b][1,2,4]triazole derivatives were synthesized and evaluated for activity as angiotensin II receptor antagonists. Molecules with the (methylbiphenylyl)tetrazole moiety at N-5 were the preferred compounds. Ethyl substitutions
