99347-21-4 Usage
Uses
Used in Pharmaceutical and Agrochemical Synthesis:
5-AMINO-1-METHYL-1H-PYRAZOLE-4-CARBOHYDRAZIDE is used as a building block for the development of new pharmaceuticals and agrochemicals, leveraging its chemical properties to create a variety of compounds with potential therapeutic and agricultural benefits.
Used in Organic Chemistry Research and Development:
In the field of organic chemistry, 5-AMINO-1-METHYL-1H-PYRAZOLE-4-CARBOHYDRAZIDE is used as a reagent in various chemical reactions, contributing to the advancement of scientific knowledge and the discovery of novel chemical processes.
Used in Biotechnology:
5-AMINO-1-METHYL-1H-PYRAZOLE-4-CARBOHYDRAZIDE has potential applications in biotechnology, where it may be employed in the development of new technologies and processes that leverage its unique chemical structure and properties.
Used in Materials Science:
In materials science, 5-AMINO-1-METHYL-1H-PYRAZOLE-4-CARBOHYDRAZIDE may be utilized in the creation of new materials with specific properties, such as those with enhanced stability, reactivity, or other desirable characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 99347-21-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,3,4 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 99347-21:
(7*9)+(6*9)+(5*3)+(4*4)+(3*7)+(2*2)+(1*1)=174
174 % 10 = 4
So 99347-21-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H9N5O/c1-10-4(6)3(2-8-10)5(11)9-7/h2H,6-7H2,1H3,(H,9,11)
99347-21-4Relevant academic research and scientific papers
Synthesis and herbicidal activities of a series of di(aminopyrazoly) ketone derivatives
Li, Jun-Fei,Zhu, You-Quan,Wang, Xin,Yang, Hua-Zheng
, p. 749 - 755 (2008/03/29)
(Chemical Equation Presented) In order to obtain new lead compounds with high herbicidal activity, a series of 5-amino pyrazole derivatives were designed and synthesized using a series of relational synthons. Their structures were determined by IR, 1H NMR, and elemental analyses. These compounds were screened for herbicidal activities against rape and barnyard grass. Their structure-activity relationships are discussed.
Heterocyclic β-Enamino Esters, 39. - Synthesis of 1H-Pyrazolopyrimidines
Wamhoff, Heinrich,Ertas, Muemtaz,Atta, Sanaa M. S.
, p. 1910 - 1916 (2007/10/02)
Die Pyrazol-Enaminoester 1a, b und 4-Pyrazolcarbohydrazide 4a, b sind nuetzliche Ausgangsverbindungen fuer die Darstellung von 1H-Pyrazolopyrimidinen.So ergeben Orthoameisensaeure- und Orthoessigsaeure-triethylester mit 4a, b die 5-(Ethoxymethylena
