111423-08-6

Usage

Molecular Structure

Contains a benzothieno[2,3-d]pyrimidin-4(3H)-one core with a 4-chlorophenyl group and a sulfanyl group attached at specific positions

Potential Activity

May have pharmacological or biological activity due to its unique structure

Potential Uses

Could be of interest for medicinal chemistry research

Further Study

Properties and potential uses need to be studied and characterized through appropriate scientific methods and testing

Upstream product

• 4506-71-2 ethyl 2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate 
• 705-69-1 N-(4-chlorophenyl)-S-methyldithiocarbamate 
• 126105-68-8 4-imino-2-thioxo-1,2,5,6,7,8-tetrahydro-4H-benzothieno<2,3-d><1,3>thiazine 
• 2131-55-7 4-Chlorophenyl isothiocyanate 
• 5936-58-3 2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylic acid 
• 111423-07-5 N¹-(3-carbethoxy-4,5,6,7-tetrahydrobenzothien-2-yl)-N²-p-chlorophenylthiourea 
• 4651-91-6 3-cyano-2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene 
• 126105-73-5 3-(4-Chloro-phenyl)-4-imino-3,4,5,6,7,8-hexahydro-1H-benzo[4,5]thieno[2,3-d]pyrimidine-2-thione 

Downstream Products

• 934246-66-9 3-(4-chlorophenyl)-2-hydrazino-5,6,7,8-tetrahydrobenzo(b)thiophene[2,3-d]pyrimidine-4(3H)-one 
• 1228467-86-4 3-(4-chlorophenyl)-2-butylthio-5,6,7,8-tetrahydrobenzothieno[2,3-d]-pyrimidin-4(3H)-one 
• 1228467-85-3 3-(4-chlorophenyl)-2-ethylthio-5,6,7,8-tetrahydrobenzothieno[2,3-d]-pyrimidin-4(3H)-one 
• 499102-66-8 3-(4-chlorophenyl)-2-(phenylmethyl)thio-5,6,7,8-tetrahydrobenzothieno[2,3-d]pyrimidin-4(3H)-one 
• 592537-53-6 3-(4-chlorophenyl)-2-propylthio-5,6,7,8-tetrahydrobenzothieno[2,3-d]-pyrimidin-4(3H)-one 
• 1132092-12-6 3-(4-chlorophenyl)-2-(ethoxycarbonylmethyl)thio-5,6,7,8-tetrahydrobenzothieno[2,3-d]pyrimidin-4(3H)-one 
• 1228467-84-2 3-(4-chlorophenyl)-2-methylthio-5,6,7,8-tetrahydrobenzothieno[2,3-d]-pyrimidin-4(3H)-one 
• 843624-33-9 4-(chlorophenyl)-1-mercapto-6,7,8,9-tetrahydrobenzo[b]thieno[2,3-b][1,2,4]triazolo[3,4-b]pyrimidin-5(4H)-one 

Relevant academic research and scientific papers

A facile microwave-assisted synthesis of some fused pyrimidine derivatives

The highly accelerated synthesis of thienopyrimidinones, theino- pyrimidines, thioxotheinopyrimidinones and a thienotriazolopyrimidinone derivatives under microwave irradiation is reported. Compared to conventional conditions, microwaves method offered se

Facile synthesis of 2-alkylthio-5,6,7,8-tetrahydrobenzothieno[2,3-d]- Pyrimidin-4(3H)-ones

Isothiocyanate 2, obtained from aza-Wittig reaction of iminophosphorane 1 with CS2, reacted with amine to give 2-thioxo-2,3,5,6,7,8- hexahydrobenzothieno[2,3-d]pyrimidin-4(1H)-ones 4 in the presence of sodium ethoxide. S-Alkylation of 4 produced 2-alkylth

Synthesis, characterization and biological studies of some novel thieno[2,3-d]pyrimidines

Several 2-unsubstituted thieno[2,3-d]pyrimidines have been prepared from 2-aminothiophene-3-carboxylic acid esters and their carbonitrile analogs. Some triazolothienopyrimidine and 2-thioxothienopyrimidine representatives have also been synthesized using

Structure-activity relationship analysis of a novel necroptosis inhibitor, Necrostatin-5

Necrostatin-5 (Nec-5) is a novel potent small-molecule inhibitor of necroptosis structurally distinct from previously described Necrostatin-1 (Nec-1), and therefore, represents a new direction for the inhibition of this cellular caspase-independent necrot

Synthesis of some thienopyrimidine derivatives

Thioxothienopyrimidinones, alkylthio- and arylalkylthiothienopyrimidinones, thienopyrimidinones, thienopyrimidines a thienopyrimidinedione and a thienotriazolopyrimidinone were prepared from 2-amino-3-carboethoxy-4,5- disubstituted thiophenes and 2-amino-

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

METHYL N-ARYLDITHIOCARBAMATES: USEFUL REAGENTS FOR THE ANNELATION OF PYRIMIDINES AND 1,3-OXAZINES TO FIVE-MEMBERED HETEROCYCLIC RINGS

The reaction of methyl N-aryldithiocarbamates with ?-excessive heteroaromatic o-amino acid derivatives leads to the annelation of 4-oxo-2-thioxopyrimidines, 2,4-dioxopyrimidines or 2-arylamino-1,3-oxazines, depending on the reaction conditions.