59898-59-8

Usage

InChI:InChI=1/C9H10N2OS2/c1-4-5(2)14-7-6(4)8(12)11(3)9(13)10-7/h1-3H3,(H,10,13)

Upstream product

• 59898-39-4 4,5-dimethyl-2-(3-methyl-thioureido)-thiophene-3-carboxylic acid ethyl ester 
• 4651-94-9 2-amino-4,5-dimethylthiophene-3-carbonitrile 
• 4815-24-1 2-amino-4,5-dimethyl-3-thiophenecarboxylic acid ethyl ester 
• 556-61-6 methyl thioisocyanate 
• 126105-83-7 4-Imino-3,5,6-trimethyl-3,4-dihydro-1H-thieno[2,3-d]pyrimidine-2-thione 

Downstream Products

• 59898-73-6 (3,5,6-trimethyl-4-oxo-3,4-dihydro-thieno[2,3-d]pyrimidin-2-ylsulfanyl)-acetic acid 

Relevant academic research and scientific papers

Interaction of heterothiocumulenes with 2-amino-3-cyanothiophenes: Formation of thienopyrimidines

Thieno-fused(1,3)-thiazine, 4-imino-2-thioxo-2,4-dihydro-1H-thieno(1,3)-thiazine (2) has been directly synthesised by the reaction of o-aminonitrile (1a) with carbon disulphide.Thiazine (2) on reaction with primary aromatic amines leads to thieno2

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.