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1H-Pyrazole-5-carboxylic acid,1-ethyl-(9CI) is a chemical compound with the formula C6H8N2O2 and a molecular weight of 140.141 g/mol. It belongs to the pyrazoles category and is characterized by a five-membered heterocyclic ring structure. Pyrazole derivatives are known for their wide-range bioactivities and are utilized in medicinal chemistry.

400755-43-3

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400755-43-3 Usage

Uses

Used in Pharmaceutical Industry:
1H-Pyrazole-5-carboxylic acid,1-ethyl-(9CI) is used as a building block for the synthesis of various pharmaceutical compounds due to its versatile chemical structure and potential bioactivities.
Used in Medicinal Chemistry Research:
1H-Pyrazole-5-carboxylic acid,1-ethyl-(9CI) is used as a research compound for exploring its potential applications in medicinal chemistry, including the development of new drugs and therapeutic agents.
Used in Chemical Synthesis:
1H-Pyrazole-5-carboxylic acid,1-ethyl-(9CI) is used as an intermediate in the synthesis of other complex organic compounds, particularly those with potential applications in the pharmaceutical and chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 400755-43-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,0,7,5 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 400755-43:
(8*4)+(7*0)+(6*0)+(5*7)+(4*5)+(3*5)+(2*4)+(1*3)=113
113 % 10 = 3
So 400755-43-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H8N2O2/c1-2-8-5(6(9)10)3-4-7-8/h3-4H,2H2,1H3,(H,9,10)

400755-43-3Relevant academic research and scientific papers

Electrosynthesis of 4-chloropyrazolecarboxylic acids

Lyalin,Petrosyan,Ugrak

experimental part, p. 291 - 296 (2010/07/09)

4-Chlorosubstituted pyrazolecarboxylic acids were synthesized via chlorination of the corresponding acids at the Pt anode in NaCl aqueous solutions under conditions of divided galvanostatic electrolysis. The efficiency of the process depends on the structures of the initial pyrazolecarboxylic acids, particularly, on the donor-acceptor properties of the substituents and on their position in the pyrazole ring. The yields of the 4-chlorosubstituted products of chlorination of pyrazole-3(5)-carboxylic acid, 1-methylpyrazole-5- carboxylic acid, 1-methyl-pyrazole-3-carboxylic acid, 1-ethylpyrazole-3- carboxylic acid, and 1-methyl-3-nitropyrazole- 5-carboxylic acid are 92, 93, 69, 80, and 4%, respectively.

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