51486-13-6

Usage

Uses

Used in Pharmaceutical Research and Development:
Ethyl 2-[(methylcarbamothioyl)amino]-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate is used as a chemical intermediate for the synthesis of new drugs and medications. Its unique structure and properties make it a promising candidate for the development of pharmaceuticals with novel therapeutic effects.
Used in Agrochemicals:
In the agrochemical industry, ethyl 2-[(methylcarbamothioyl)amino]-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate may be used as a component in the formulation of pesticides or other agricultural chemicals. Its potential applications in this field could include enhancing the effectiveness of existing products or contributing to the development of new, more targeted agrochemicals.
Used in Industrial Processes:
Ethyl 2-[(methylcarbamothioyl)amino]-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate may also find applications in various industrial processes. Its specific uses in this context will depend on the results of further research and testing, but it could potentially be employed as a catalyst, a reagent, or a component in the production of other chemicals or materials.

Upstream product

• 4506-71-2 ethyl 2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate 
• 556-61-6 methyl thioisocyanate 

Downstream Products

• 38201-61-5 3-methyl-2-thioxo-2,3,5,6,7,8-hexahydro-1H-benzo[4,5]thieno[2,3-d]pyrimidin-4-one 
• 38201-61-5 3-Methyl-2-thioxo-2,3,5,6,7,8-hexahydro-1H-benzo[4,5]thieno[2,3-d]pyrimidin-4-one 
• 59898-79-2 (3-methyl-4-oxo-3,4,5,6,7,8-hexahydro-benzo[4,5]thieno[2,3-d]pyrimidin-2-ylsulfanyl)-acetic acid ethyl ester 
• 59898-74-7 (3-methyl-4-oxo-3,4,5,6,7,8-hexahydro-benzo[4,5]thieno[2,3-d]pyrimidin-2-ylsulfanyl)-acetic acid 
• 79587-91-0 (3-Methyl-4-oxo-3,4,5,6,7,8-hexahydro-benzo[4,5]thieno[2,3-d]pyrimidin-2-ylsulfanyl)-phenyl-acetic acid 
• 79598-26-8 3a-Ethoxy-4-methyl-2-phenyl-3a,4,6,7,8,9-hexahydro-3,10-dithia-4,10b-diaza-cyclopenta[a]fluorene-1,5-dione 

Relevant academic research and scientific papers

Synthesis and pharmacological activities of some 3-substituted thienopyrimidin-4-one-2-thiones

The condensation of substituted 2-amino-3-carbethoxy-thiophenes with methyl, ethyl and phenyl isothiocyanate yields the corresponding thienylthioureas which cyclize in ethanol saturated with dry hydrochloric acid to form 3-substituted thienopyrimid

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

Studies on Fused-ring Mesoionic Thiazolothienopyrimidine Systems

Cyclodehydration of 2-carboxymethylmercaptothienopyrimidin-4(3H)-ones (IV) have been studied.IV (R3=R4=Ph and R3=Me,R4=Ph) on reaction with acetic anhydride and pyridine mixture readily yield stable fusedring mesoionic systems (VI).While IV (R3=Ph,

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.