59898-45-2

Basic information

• Product Name: 4,5-dimethyl-2-(3-phenyl-thioureido)-thiophene-3-carboxylic acid ethyl ester
• Synonyms: 4,5-dimethyl-2-(3-phenyl-thioureido)-thiophene-3-carboxylic acid ethyl ester
• CAS NO: 59898-45-2
• Molecular Weight: 334.463
• Mol File: 59898-45-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4,5-dimethyl-2-(3-phenyl-thioureido)-thiophene-3-carboxylic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4,5-dimethyl-2-(3-phenyl-thioureido)-thiophene-3-carboxylic acid ethyl ester(59898-45-2)
• EPA Substance Registry System: 4,5-dimethyl-2-(3-phenyl-thioureido)-thiophene-3-carboxylic acid ethyl ester(59898-45-2)

Safety Data

• Hazardous Substances Data: 59898-45-2(Hazardous Substances Data)

Upstream product

• 103-72-0 phenyl isothiocyanate 
• 4815-24-1 2-amino-4,5-dimethyl-3-thiophenecarboxylic acid ethyl ester 

Downstream Products

• 79587-86-3 (5,6-Dimethyl-4-oxo-3-phenyl-3,4-dihydro-thieno[2,3-d]pyrimidin-2-ylsulfanyl)-acetic acid 
• 112101-03-8 5,6-Dimethyl-2-phenylamino-thieno<2,3-d><1,3>thiazin-4-thion 
• 105544-46-5 5,6-Dimethyl-2-phenylamino-thieno-<2,3-d><1,3>thiazin-4-on 
• 59898-64-5 5,6-Dimethyl-3-phenyl-2-thioxo-2,3-dihydro-1H-thieno[2,3-d]pyrimidin-4-one 

Relevant articles and documents

The Facile Synthesis of 2-Aminothienothiazin-4-ones, in Some Cases 5,6-Anelated

The cyclization of ethyl 2-thioureidothiophene-3-carboxylates is known to give 2-thioxothienopyrimidin-4-ones not only under basic conditions but also upon treatment with ethanolic hydrochloric acid.On the other hand, we have found that ethyl 2-thi

Synthesis of 3 substituted thieno[2,3 d]pyrimidin 4(3H) one 2 mercaptoacetic acids and their ethyl esters for pharmacological screening

3 Substituted thieno[2,3 d]pyrimidin 4(3H) one 2 mercaptoacetic acids and their ethyl esters were synthesized from 2 mercaptothieno[2,3 d]pyrimidin 4 (3H) ones, which were obtained by cyclization of thienylthioureas in acidic medium. Analgesic, anti inflammatory, and anticonvulsant activities were found in some of these compounds. Significant antimicrobial activity was exhibited by thienylthioureas.