17355-75-8

Basic information

• Product Name: 1H-Pyrazole-3-carboxylic acid, 1,5-diphenyl-, ethyl ester
• Synonyms: 1H-Pyrazole-3-carboxylic acid, 1,5-diphenyl-, ethyl ester;ethyl 1,5-diphenyl-1H-pyrazole-3-carboxylate
• CAS NO: 17355-75-8
• Molecular Formula: C₁₈H₁₆N₂O₂
• Molecular Weight: 292.33184
• Mol File: 17355-75-8.mol
• Article Data: 17

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1H-Pyrazole-3-carboxylic acid, 1,5-diphenyl-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrazole-3-carboxylic acid, 1,5-diphenyl-, ethyl ester(17355-75-8)
• EPA Substance Registry System: 1H-Pyrazole-3-carboxylic acid, 1,5-diphenyl-, ethyl ester(17355-75-8)

Safety Data

• Hazardous Substances Data: 17355-75-8(Hazardous Substances Data)

Usage

Belongs to the pyrazole family

This compound is part of a group of organic compounds that contain a five-membered ring with one nitrogen atom.

Ester derivative

This compound is formed by the esterification of the carboxylic acid group of 1,5-diphenyl-1H-pyrazole-3-carboxylic acid with ethanol.

Applications in organic synthesis, drug development, and material science

This compound may be used as a building block or intermediate in the synthesis of more complex molecules, or as a potential drug candidate due to its biological activity.

Specific properties and potential uses depend on its synthesis and purification

The properties and potential uses of this compound may vary depending on the method of synthesis and the degree of purity achieved.

Proper handling and safety precautions

As with any chemical compound, it is important to handle 1H-Pyrazole-3-carboxylic acid, 1,5-diphenyl, ethyl ester with care and follow appropriate safety protocols to minimize the risk of exposure or accidents.

Upstream product

• 6296-54-4 ethyl 2,4-dioxo-4-phenylbutyrate 
• 100-63-0 phenylhydrazine 
• 70-11-1 α-bromoacetophenone 
• 80447-71-8 phenylhydrazone of ethyl ester of glyoxalic acid 
• 3453-00-7 diethyl benzoylmethylphosphonate 
• 28663-68-5 ethyl (phenylhydrazono)chloroacetate 
• 98-86-2 acetophenone 
• 88330-79-4 2-hydroxy-4-oxo-4-phenylbut-2-enoic acid ethyl ester 
• 64-17-5 ethanol 
• 1032273-54-3 4-bromo-4,4-difluoro-1-phenylbutane-1,3-dione 
• 3815-83-6 3,4-diphenylsydnone 
• 623-47-2 propynoic acid ethyl ester 
• 6919-61-5 N-methoxy-N-methylbenzamide 
• 907178-38-5 (E)-2-(N-methoxy-N-methyl-amino)-4-oxo-4-phenyl-2-butenoic acid ethyl ester 

Downstream Products

• 1428261-49-7 C₃₂H₄₅N₃O 
• 1428261-50-0 C₂₁H₂₂N₄O 
• 1428261-48-6 C₃₄H₄₇N₃O 

Relevant articles and documents

Synthesis and Biological Screening of Novel 5-(5-Aryl-1-phenyl-1H-pyrazol-3-yl)-3-aryl-1,2,4-oxadiazole Derivatives

A new series of 5-(5-aryl-1-phenyl-1H-pyrazol-3-yl)-3-aryl-1,2,4-oxadiazole (6a-o) have been synthesized by a cyclocondensation reaction of ethyl 5-(4-chlorophenyl)-1-phenyl-1H-pyrazole-3-carboxylate (3a-c) with aryl imidoxime (5a-e). The newly synthesize

Discovery of 1,5-Diphenylpyrazole-3-Carboxamide Derivatives as Potent, Reversible, and Selective Monoacylglycerol Lipase (MAGL) Inhibitors

Monoacylglycerol lipase (MAGL) is a serine hydrolase that plays an important role in the degradation of the endocannabinoid neurotransmitter 2-arachidonoylglycerol, which is implicated in many physiological processes. Beyond the possible utilization of MA

A new efficient synthesis of pyrazoles from hydrazonoyl halides and β-oxophosphonates

A new practical and efficient synthesis of 1,3,5-trisubstituted pyrazoles has been developed by reacting of hydrazonoyl halides with β-oxophosphonates under mild conditions in good yields with excellent regioselectivity. This process employs an addition-elimination sequence. Wide scope, functional group compatibility has been established.