40745-03-7

Basic information

• Product Name: 5-aMino-3-Methylthio-1-phenyl-1H-pyrazole-4-carboxylic acid ethyl ester
• Synonyms: 5-aMino-3-Methylthio-1-phenyl-1H-pyrazole-4-carboxylic acid ethyl ester;Ethyl 5-aMino-3-(Methylthio)-1-phenyl-1H-pyrazole-4-carboxylate
• CAS NO: 40745-03-7
• Molecular Formula: C₁₃H₁₅N₃O₂S
• Molecular Weight: 277.3421
• Mol File: 40745-03-7.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5-aMino-3-Methylthio-1-phenyl-1H-pyrazole-4-carboxylic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 5-aMino-3-Methylthio-1-phenyl-1H-pyrazole-4-carboxylic acid ethyl ester(40745-03-7)
• EPA Substance Registry System: 5-aMino-3-Methylthio-1-phenyl-1H-pyrazole-4-carboxylic acid ethyl ester(40745-03-7)

Safety Data

• Hazardous Substances Data: 40745-03-7(Hazardous Substances Data)

Upstream product

• 100-63-0 phenylhydrazine 
• 105-56-6 ethyl 2-cyanoacetate 
• 17823-58-4 ethyl 2-cyano-3,3-di(methylsulfanyl)acrylate 
• 54417-51-5 ethyl 5?amino?3?(methylthio)?1H?pyrazole?4?carboxylate 

Downstream Products

• 117480-66-7 5-chloroacetylamino-3-methylsulfanyl-1-phenyl-1H-pyrazole-4-carboxylic acid ethyl ester 
• 158095-23-9 5-amino-4-carboxyl-3-methylthio-1-phenylpyrazole 
• 750598-28-8 C₃₁H₂₈N₃O₂PS 
• 954146-46-4 6-(4-bromo-phenyl)-5-(4-chloro-phenyl)-3-methylsulfanyl-1-phenyl-1,5-dihydro-pyrazolo[3,4-d]pyrimidin-4-one 
• 947238-78-0 5-amino-3-(methylthio)-1-phenyl-1H-pyrazole-4-carbohydrazide 
• 776298-90-9 3-methylsulfanyl-1-phenyl-5-phenyliminomethyleneamino-1H-pyrazole-4-carboxylic acid ethyl ester 
• 776298-91-0 3-methylsulfanyl-1-phenyl-5-(N'-phenyl-N''-propyl-guanidino)-1H-pyrazole-4-carboxylic acid ethyl ester 

Relevant articles and documents

Synthesis and pharmacological investigation of 5-substituted-3- methylsulfanyl-1 H-pyrazole-4-carboxylic acid ethyl esters as new analgesic and anti-inflammatory agents

Purpose: To synthesize a new series of 5-substituted-3-methylsulfanyl-1H- pyrazole-4-carboxylic acid ethyl esters for their analgesic and anti-inflammatory activity. Methods: The title compound synthesized by reacting the amino group of 5-amino-3-methylsu