77556-50-4 Usage
Uses
Used in Medicinal Chemistry:
1-Pyridin-2-yl-1H-pyrazole-4-carboxylic acid is used as a key intermediate in the synthesis of various bioactive molecules for drug development. Its unique structure and properties make it a valuable building block for creating more complex chemical compounds with potential therapeutic applications.
Used in Enzyme Inhibition:
1-Pyridin-2-yl-1H-pyrazole-4-carboxylic acid is studied for its potential role as an enzyme inhibitor. Its ability to interact with specific enzymes may lead to the development of new drugs targeting various diseases and conditions.
Used in Antimicrobial Applications:
1-Pyridin-2-yl-1H-pyrazole-4-carboxylic acid has been studied for its antimicrobial properties. Its potential to inhibit the growth of certain microorganisms makes it a candidate for the development of new antimicrobial agents to combat drug-resistant infections.
Used in Pharmaceutical Industry:
1-Pyridin-2-yl-1H-pyrazole-4-carboxylic acid is used as a compound of interest in the pharmaceutical industry for its potential applications in drug development. Its unique structure and properties contribute to the discovery and design of new therapeutic agents.
Used in Agrochemical Industry:
1-Pyridin-2-yl-1H-pyrazole-4-carboxylic acid is also used in the agrochemical industry, where its potential applications in the development of new pesticides or herbicides can contribute to more effective and targeted agricultural solutions.
Check Digit Verification of cas no
The CAS Registry Mumber 77556-50-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,5,5 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 77556-50:
(7*7)+(6*7)+(5*5)+(4*5)+(3*6)+(2*5)+(1*0)=164
164 % 10 = 4
So 77556-50-4 is a valid CAS Registry Number.
77556-50-4Relevant academic research and scientific papers
NITROGEN-CONTAINING HETEROARYL DERIVATIVES
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Page/Page column 40-41, (2011/08/06)
The invention is concerned with novel nitrogen-containing heteroaryl derivatives of formula (I) wherein R1, R2, R3, R4, R5, A1, A2, and Y are as defined in the description and in
NITROGEN-CONTAINING HETEROARYL DERIVATIVES
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Page/Page column 96, (2011/08/08)
The invention is concerned with novel nitrogen-containing heteroaryl derivatives of formula (I) wherein R1, R2, R3, R4, R5, A1, A2, and Y are as defined in the description and in
Certain pyrazoline derivatives with kinase inhibitory activity
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Page/Page column 100-101, (2008/12/06)
The present invention provides certain pyrazoline compounds useful as inhibitors of protein kinases. The invention also provides pharmaceutical compositions and methods of using the compositions in the treatment of various diseases.
Design and synthesis of a series of novel pyrazolopyridines as HIF 1-α prolyl hydroxylase inhibitors
Warshakoon, Namal C.,Wu, Shengde,Boyer, Angelique,Kawamoto, Richard,Renock, Sean,Xu, Kevin,Pokross, Matthew,Evdokimov, Artem G.,Zhou, Songtao,Winter, Carol,Walter, Richard,Mekel, Marlene
, p. 5687 - 5690 (2007/10/03)
Recently resolved X-ray crystal structure of HIF-1α prolyl hydroxylase was used to design and develop a novel series of pyrazolopyridines as potent HIF-1α prolyl hydroxylase inhibitors. The activity of these compounds was determined in a human EGLN-1 assa
Hetarylyrazoles. II. Reactions of Pyrazol-1'-ylpyridines
Khan, Misbahul Ain,Pinto, Alvaro Augusto Alves
, p. 9 - 14 (2007/10/02)
Pyrazol-1'-ylpyridines undergo electrophilic substitution reactions (bromination, chlorination and nitration) preferentially in the pyrazole ring.There is some evidence of the mutual influence of the pyrazole and the pyridine ring on the reactivity of the
