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4-(Pyridin-2-yl)-1H-pyrazole-3-carboxylic acid is a heterocyclic compound that features a pyridine ring and a pyrazole ring connected to a carboxylic acid group. 4-(Pyridin-2-yl)-1H-pyrazole-3-carboxylicacid is notable for its potential applications in medicinal chemistry and pharmaceutical research, owing to its multiple functional groups that can be tailored to produce new derivatives with a range of biological activities. Additionally, it is recognized for its utility as a ligand in coordination chemistry and as a precursor for synthesizing more complex organic compounds, making it a valuable component in the development of innovative drugs and materials within the realm of organic chemistry.

1260765-26-1

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1260765-26-1 Usage

Uses

Used in Medicinal Chemistry and Pharmaceutical Research:
4-(Pyridin-2-yl)-1H-pyrazole-3-carboxylic acid is utilized as a building block for the creation of new drug candidates due to its ability to be modified into various derivatives with diverse biological activities. Its presence in heterocyclic structures makes it a promising candidate for the development of pharmaceuticals with novel therapeutic properties.
Used in Coordination Chemistry:
As a ligand, 4-(Pyridin-2-yl)-1H-pyrazole-3-carboxylic acid is employed in coordination chemistry to form complexes with metal ions. This application is significant for the study of metal-organic frameworks and the development of new materials with specific properties, such as catalysis or sensing.
Used in Organic Synthesis:
4-(Pyridin-2-yl)-1H-pyrazole-3-carboxylic acid serves as a precursor in the synthesis of more complex organic compounds. Its structural features allow for the construction of a variety of molecules that can be further explored for their potential applications in various fields, including but not limited to pharmaceuticals, agrochemicals, and materials science.
Used in Drug Development:
4-(Pyridin-2-yl)-1H-pyrazole-3-carboxylic acid is used as a starting material for the development of new drugs. Its versatile chemical structure allows for the design of molecules with specific target interactions, potentially leading to the discovery of new therapeutic agents with improved efficacy and selectivity.

Check Digit Verification of cas no

The CAS Registry Mumber 1260765-26-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,7,6 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1260765-26:
(9*1)+(8*2)+(7*6)+(6*0)+(5*7)+(4*6)+(3*5)+(2*2)+(1*6)=151
151 % 10 = 1
So 1260765-26-1 is a valid CAS Registry Number.

1260765-26-1Downstream Products

1260765-26-1Relevant articles and documents

Preparations of 4-substituted 3-carboxypyrazoles

Janin, Yves L.

, p. 1410 - 1414 (2013)

The scopes of three synthetic methods reported for the preparation of an array of 3-pyrazolecarboxylates featuring substituents on position 4 were investigated. The first one is based on the potassium permanganate oxidation of methylpyrazoles. The second starts with the condensation between DMF dimethylacetal and ethyl pyruvate and is followed by the addition of hydrazine hydrochloride. The last one makes use of the cycloaddition of diazomethane on acrylate esters followed by a bromine-based oxidative rearrangement into 4-substituted 3-pyrazole esters.

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