931-08-8 Usage
Uses
Used in Pharmaceutical Industry:
1H-pyrazole-1-carboxamide is used as a building block for the synthesis of various biologically active compounds, including potential drug candidates. Its unique structure and properties make it a valuable component in the development of new medications.
Used in Agrochemical Industry:
1H-pyrazole-1-carboxamide is used as a key intermediate in the production of agrochemicals, contributing to the development of effective pesticides and other agricultural chemicals.
Used in Materials Science:
1H-pyrazole-1-carboxamide is used in the research and development of new materials, thanks to its potential to form various chemical structures and interactions.
Used in Biochemical Research:
1H-pyrazole-1-carboxamide is used as an enzyme inhibitor, making it a valuable tool in biochemical research for studying enzyme functions and developing targeted therapies.
Overall, 1H-pyrazole-1-carboxamide is a valuable and versatile chemical with diverse potential applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 931-08-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 931-08:
(5*9)+(4*3)+(3*1)+(2*0)+(1*8)=68
68 % 10 = 8
So 931-08-8 is a valid CAS Registry Number.
931-08-8Relevant academic research and scientific papers
Synthesis of 1-Oxo-1H-pyrazolotriazol-4-ium-3-olates. - A Ring-Chain Tautomerism in the Series of Bicyclic Dipolar Heterocycles
Boettcher, Andreas,Debaerdemaeker, Tony,Radziszewski, Juliusz G.,Friedrichsen, Willy
, p. 895 - 908 (2007/10/02)
1-(Trimethylsilyl)pyrazole (12) reacts with chlorocarbonyl isocyanate to give a compound, which - dependent on the state of aggregation - may exist both as a bicyclic dipolar heterocycle (7) and as monocyclic 1-pyrazolyl carbonyl isocyanate (8).Methyl-substituted derivatives (19a, b) show a similar behaviour.MNDO calculations for the parent systems (7, 8) are in accord with these experimental observations.The structure of 5,6,7-trimethyl-1-oxo-1H-pyrazolotriazol-4-ium-3-olate (19b) has been clarified by X-ray analysis.
