76053-69-5

Upstream product

• 40017-83-2 3-(2-Nitrophenyl)-3-oxopropionsaeurenitril 
• 123-38-6 propionaldehyde 

Downstream Products

• 76054-15-4 1,7-Dimethyl-6-nitro-5-(2-nitro-phenyl)-1,3-dihydro-thieno[2,3-e][1,4]diazepin-2-one 
• 76054-10-9 7-Methyl-6-nitro-5-(2-nitro-phenyl)-1,3-dihydro-thieno[2,3-e][1,4]diazepin-2-one 
• 76053-90-2 2-Amino-N-[5-methyl-3-(2-nitro-benzoyl)-thiophen-2-yl]-acetamide 
• 76053-82-2 2-Iodo-N-[5-methyl-3-(2-nitro-benzoyl)-thiophen-2-yl]-acetamide 
• 76054-03-0 1,7-Dimethyl-5-(2-nitro-phenyl)-1,3-dihydro-thieno[2,3-e][1,4]diazepin-2-one 
• 76053-97-9 7-Methyl-5-(2-nitro-phenyl)-1,3-dihydro-thieno[2,3-e][1,4]diazepin-2-one 
• 76053-75-3 2-Chloro-N-[5-methyl-3-(2-nitro-benzoyl)-thiophen-2-yl]-acetamide 

Relevant academic research and scientific papers

Temperature-Controlled Thiation of α-Cyano-β-Alkynyl Carbonyl Derivatives for de Novo Synthesis of 2-Aminothiophenes and Thieno[2,3- c]isothiazoles

Making use of temperature-controlled thiation as a key operation, a simple route to 2-aminothiophenes or thieno[2,3-c]isothiazoles has been newly developed wherein the 2-aminothiophene nucleus was formed through an initial formation of thioamide followed