78984-83-5

Usage

InChI:InChI=1/C11H12ClNO2/c1-8(14)6-11(15)13-7-9-2-4-10(12)5-3-9/h2-5H,6-7H2,1H3,(H,13,15)

Upstream product

• 674-82-8 4-methyleneoxetan-2-one 
• 65560-92-1 Ammonium-(4-chlorbenzyl)-dithiocarbamat 
• 104-86-9 4-chlorobenzylamine 

Downstream Products

• 1253058-96-6 3-methylquinoxaline-2-carboxylic acid p-chlorobenzylamide 1,4-di-N-oxide 
• 1253058-99-9 6,7-dichloro-3-methylquinoxaline-2-carboxylic acid p-chlorobenzylamide 1,4-di-N-oxide 
• 1253058-98-8 3,7-dimethylquinoxaline-2-carboxylic acid p-chlorobenzylamide 1,4-di-N-oxide 
• 1253058-97-7 7-chloro-3-methylquinoxaline-2-carboxylic acid p-chlorobenzylamide 1,4-di-N-oxide 
• 1439365-81-7 N-(4-chlorobenzyl)-2,2-difluoro-3-oxobutanamide 
• 1439365-87-3 C₁₁H₁₁ClFNO₂ 
• 80357-30-8 N,1-bis(4-chlorobenzyl)-2,4-dimethyl-6-oxo-1,6-dihydropyridine-3-carboxamide 

Relevant academic research and scientific papers

Synthesis and antimycobacterial activity of new quinoxaline-2-carboxamide 1,4-di-N-oxide derivatives

As a continuation of our research and with the aim of obtaining new anti-tuberculosis agents which can improve the current chemotherapeutic anti-tuberculosis treatments, forty-three new quinoxaline-2-carboxamide 1,4-di-N-oxide derivatives were synthesized

5,6-dihydroimidazo(2,1-b)thiazole-2-carboxamide derivatives or salts thereof

5,6-dihydroimidazo[2,1-b]thiazole-2-carboxamide derivatives represented by the following general formula [I] STR1 wherein R1, R2, R3 and R4 are either the same or different and mean individually a hydrogen atom or lower alkyl group, Y denotes a specific phenyl-containing substituted amino group, and their salts. These compounds have excellent immuno-modulating activities.

1,3-Thiazines, XVI: 2-Thioxotetrahydro-1,3-thiazin-4-ones by Use of β-Propiolactones, Part 2

Reactions of β-lactones with dithiocarbamates leading to 2 and cyclization of the products yielding 2-thioxo-tetrahydro-1,3-thiazin-4-ones 3 are described.With derivatives of diketene (β-propiolactones with exocyclic double bonds) no 1,3-thiazines 6 are obtained.Instead, the amides of β-ketoacids 7 are formed with the elimination of carbon disulfide.