93282-12-3

Upstream product

• 7291-01-2 N,N-dimethyl-4-nitrobenzamide 

Downstream Products

• 946-46-3 4-Nitrothiobenzoesaeure-O-ethylester 
• 15563-48-1 N,N-dimethyl-p-nitro-thiobenzamide 
• 946-47-4 ethyl 4-nitrobenzodithioate 
• 1649456-34-7 4-chloro-2-(4-nitrophenyl)-5,6-dihydro[1]benzoxepino[5,4-d]pyrimidine 
• 1649456-45-0 4-morpholino-2-(4-nitrophenyl)-5,6-dihydro[1]benzoxepino[5,4-d]pyrimidine 
• 1649456-53-0 4-ethylamino-2-(4-nitrophenyl)-5,6-dihydro[1]benzoxepino[5,4-d]pyrimidine 
• 1649456-61-0 4-(2-hydroxyethylamino)-2-(4-nitrophenyl)-5,6-dihydro[1]benzoxepino[5,4-d]pyrimidine 
• 1649456-69-8 4-(N-methyl-2-hydroxyethylamino)-2-(4-nitrophenyl)-5,6-dihydro[1]benzoxepino[5,4-d]pyrimidine 

Relevant academic research and scientific papers

Synthesis and Crystal Structures of Stable 4-Aryl-2-(trichloromethyl)-1,3-diaza-1,3-butadienes

A simple and convenient method to generate 4-aryl-substituted 1H-2-(trichloromethyl)-1,3-diaza-1,3-butadienes from aryl(chloro)methaniminium salts (best known as Vilsmeier-Haack reagents) and trichloroacetamidine has been developed. These 4-aryl-1H-1,3-di

Polycyclic N-heterocyclic compounds. Part 75: Synthesis of 2,4-disubstituted 5,6-dihydro[1]benzoxepino[5,4-d]pyrimidines and 12-substituted 1,2,4,5-tetrahydro[1]benzoxepino[4,5-e]imidazo[1,2-c]pyrimidines as potential antiplatelet aggregators

Libraries of tricyclic 2-substituted 4-alkylamino-5,6-dihydro[1] benzoxepino[5,4-d]pyrimidines and tetracyclic 12-substituted 1,2,4,5-tetrahydro[1]benzoxepino[4,5-e]imidazo[1,2-c]pyrimidines were synthesized as part of our research to develop new effectiv