4815-38-7

Basic information

• Product Name: ETHYL 2-AMINO-4-METHYL-5-PHENYLTHIOPHENE-3-CARBOXYLATE
• Synonyms: 2-Amino-4-methyl-5-phenyl-3-thiophenecarboxylic acid ethyl ester;2-aMino-4-Methyl-5-phenylthiophene-3-carboxylic acid ethyl ester
• CAS NO: 4815-38-7
• Molecular Formula: C₁₄H₁₅NO₂S
• Molecular Weight: 261.34
• Mol File: 4815-38-7.mol
• Article Data: 10

Chemical Properties

• Melting Point: 95-97℃
• Boiling Point: 397.6°Cat760mmHg
• Flash Point: 194.2°C
• Appearance: /
• Density: 1.203
• Vapor Pressure: 1.57E-06mmHg at 25°C
• Refractive Index: 1.604
• Storage Temp.: 2-8°C
• CAS DataBase Reference: ETHYL 2-AMINO-4-METHYL-5-PHENYLTHIOPHENE-3-CARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 2-AMINO-4-METHYL-5-PHENYLTHIOPHENE-3-CARBOXYLATE(4815-38-7)
• EPA Substance Registry System: ETHYL 2-AMINO-4-METHYL-5-PHENYLTHIOPHENE-3-CARBOXYLATE(4815-38-7)

Safety Data

• Hazardous Substances Data: 4815-38-7(Hazardous Substances Data)

Usage

General Description

Ethyl 2-amino-4-methyl-5-phenylthiophene-3-carboxylate is a chemical compound with a molecular formula C14H15NO2S. It is a thiophene derivative with an ethyl ester functional group attached to the carboxyl group. ETHYL 2-AMINO-4-METHYL-5-PHENYLTHIOPHENE-3-CARBOXYLATE is a white to light yellow solid with a characteristic odor. It is used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. Ethyl 2-amino-4-methyl-5-phenylthiophene-3-carboxylate has potential applications in the development of new drugs and in academic research. It is important to handle this compound with care and follow safety guidelines, as direct exposure may cause irritation to the skin, eyes, and respiratory system.

InChI:InChI=1/C14H15NO2S/c1-3-17-14(16)11-9(2)12(18-13(11)15)10-7-5-4-6-8-10/h4-8H,3,15H2,1-2H3

Upstream product

• 103-79-7 1-phenyl-acetone 
• 105-56-6 ethyl 2-cyanoacetate 
• 7148-59-6 2-cyano-3-methyl-4-phenyl-crotonic acid ethyl ester 
• 6186-22-7 4-bromophenyl acetone 
• 219547-43-0 2-amino-5-(4-bromo-phenyl)-4-methyl-thiophene-3-carboxylic acid ethyl ester 

Downstream Products

• 177088-92-5 4-Chloro-5-methyl-2-methylsulfanyl-6-phenyl-thieno[2,3-d]pyrimidine 
• 177088-95-8 (5-Methyl-2-methylsulfanyl-6-phenyl-thieno[2,3-d]pyrimidin-4-yl)-hydrazine 
• 177088-96-9 9-Methyl-5-methylsulfanyl-8-phenyl-tetrazolo[1,5-c]thieno[3,2-e]pyrimidine 
• 176852-92-9 5-methyl-2-methylsulfanyl-6-phenyl-3H-thieno[2,3-d]pyrimidin-4-one 
• 1213791-94-6 ethyl 4-methyl-5-phenyl-2-(1H-pyrrol-1-yl)thiophene-3-carboxylate 
• 1213791-97-9 ethyl 2-(cyanodiazenyl)-4-methyl-5-phenylthiophene-3-carboxylate 
• 1213791-98-0 ethyl 2-chloro-4-methyl-5-phenylthiophene-3-carboxylate 
• 1213791-92-4 ethyl 2-isothiocyanato-4-methyl-5-phenylthiophene-3-carboxylate 
• 1213791-82-2 ethyl 2-acetamido-4-methyl-5-phenylthiophene-3-carboxylate 
• 1213791-84-4 ethyl 2-benzamido-4-methyl-5-phenylthiophene-3-carboxylate 
• 1213791-85-5 ethyl 2-(2-ethoxy-2-oxoacetamido)-4-methyl-5-phenylthiophene-3-carboxylate 
• 1213791-95-7 ethyl 2-(3,3-dimethyltriaz-1-enyl)-4-methyl-5-phenylthiophene-3-carboxylate 
• 1213791-91-3 ethyl 2-(2-bromoacetamido)-4-methyl-5-phenylthiophene-3-carboxylate 
• 1213791-83-3 ethyl 4-methyl-5-phenyl-2-(2,2,2-trifluoroacetamido)thiophene-3-carboxylate 

Relevant articles and documents

Unprecedented convergent synthesis of the fused tricyclic thiophenes via Friedel-Crafts cycliacylation reactions

An efficient and concise procedure toward benzo-and pyridothieno[2,3-b] fused N-heterocycles from readily available substrates is described. The process involves Lewis and Bronsted acids-mediated Friedel-Crafts cyclizations of the synthesized thiophene-ba

Processes for the production of thienopyrimidine derivatives

The present invention provides a process for producing an intermediate for thienopyrimidine derivatives having the GnRH antagonistic activity at an industrial large scale. The process for production of the present invention relates to a process for produc

Thienopyrimidine derivatives, their production and use

Thienopyrimidine derivatives are disclosed. Also disclosed are methods for the production and use of these compounds.