15943-83-6

Usage

Ethyl ester derivative

1-(4-chlorophenyl)-3-methyl-1H-pyrazole-5-carboxylic acid The compound is derived from 1-(4-chlorophenyl)-3-methyl-1H-pyrazole-5-carboxylic acid by attaching an ethyl ester group.

Pyrazole carboxylic acid

1H-Pyrazole-5-carboxylic acid, 1-(4-chlorophenyl)-3-methyl-, ethyl ester belongs to the pyrazole family, which is a five-membered heterocyclic ring system containing one nitrogen atom and one carbon atom.

Potential anti-inflammatory and analgesic activities

The compound has potential therapeutic effects, such as reducing inflammation and relieving pain, which can be useful in the development of pharmaceuticals.

Building block for synthesis of bioactive molecules

1H-Pyrazole-5-carboxylic acid, 1-(4-chlorophenyl)-3-methyl-, ethyl ester can be used as a starting material for the synthesis of various other bioactive molecules, making it a valuable tool in medicinal chemistry.

Valuable tool in medicinal chemistry and drug discovery

The compound's chemical properties and structure make it an important component in the research and development of pharmaceuticals, aiding in the discovery of new drugs and therapeutic agents.

Upstream product

• 1073-69-4 N-4-chlorophenylhydrazine 
• 615-79-2 ethyl 2,4-diketopentanoate 
• 1448684-12-5 C₁₃H₁₅ClN₂O₃ 

Downstream Products

• 1019007-88-5 C₁₁H₈Cl₂N₂O 
• 1351169-52-2 1-(4-chlorophenyl)-3-methyl-N-(1H-tetrazol-5-yl)-1H-pyrazole-5-carboxamide 
• 15943-84-7 1-(4-chlorophenyl)-3-methyl-1H-pyrazole-5-carboxylic acid 
• 1448684-55-6 2-(2-(5-fluorouracil-1-yl)acetamido)ethyl 1-(4-chlorophenyl)-3-methyl-1H-pyrazole-5-carboxylate 

Relevant academic research and scientific papers

Synthesis and insecticidal evaluation of aryl pyrazole 5-fluorouracil compounds

Twenty eight aryl pyrazole derivatives containing 5-fluorouracil were designed and synthesised via the key intermediate 1-aryl-3-methyl-1H-pyrazole-5- carboxylic acid. The structures of target compounds were confirmed by 1H NMR, FT-IR, EA and t

Microwave-assisted synthesis of tetrazolyl pyrazole amides

A rapid and efficient microwave-assisted synthesis N-(1H-tetrazol-5-yl) derivatives of 3-methyl-1-phenyl-1H-pyrazole- 5-carboxamide is described. These tetrazole pyrazole amides have interesting bacteriocidal, pesticidal, herbicidal and antimicrobial activities. They were identified by IR and 1H NMR elemental analyses. The target compounds were obtained in a shorter reaction time compared to conventional heating methods.

Functionalized 4-aminoquinolines by rearrangement of pyrazole N-heterocyclic carbenes

(Figure Presented) Thermal decarboxylation of 1-phenyl pyrazolium-3- carboxylates from the mesomeric betaine class of substances leads to pyrazole-N-heterocyclic carbenes, which immediately rearrange to multiply substituted 4-aminoquinolines (see scheme). These species are of interest for the synthesis of heterocycles and pharmacologically active compounds.