1100799-36-7

Basic information

• Product Name: 2-acetyl-3-ethoxy-N-{4-[(pyrimidin-2-ylamino)sulfonyl]phenyl}acrylamide
• Synonyms: 2-acetyl-3-ethoxy-N-{4-[(pyrimidin-2-ylamino)sulfonyl]phenyl}acrylamide
• CAS NO: 1100799-36-7
• Molecular Weight: 390.42
• Mol File: 1100799-36-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-acetyl-3-ethoxy-N-{4-[(pyrimidin-2-ylamino)sulfonyl]phenyl}acrylamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-acetyl-3-ethoxy-N-{4-[(pyrimidin-2-ylamino)sulfonyl]phenyl}acrylamide(1100799-36-7)
• EPA Substance Registry System: 2-acetyl-3-ethoxy-N-{4-[(pyrimidin-2-ylamino)sulfonyl]phenyl}acrylamide(1100799-36-7)

Safety Data

• Hazardous Substances Data: 1100799-36-7(Hazardous Substances Data)

Upstream product

• 122-51-0 orthoformic acid triethyl ester 
• 134477-88-6 3-oxo-N-{4-[(pyrimidin-2-ylamino)sulphonyl]phenyl}butanamide 

Downstream Products

• 1100799-35-6 3-methyl-N-{4-[(pyrimidin-2-ylamino)sulfonyl]phenyl}-1H-pyrazole-4-carbohydrazonamide 
• 1100799-28-7 5-cyano-2-methyl-N-{4-[(pyrimidin-2-ylamino)sulfonyl]phenyl}-6-thioxo-1,6-dihydropyridine-3-carboxamide 
• 1100799-27-6 4-(3,5-diacetyl-6-hydroxy-2-oxo-2H-pyridin-1-yl)-N-pyrimidin-2-ylbenzene-sulfonamide 
• 1100799-21-0 5-acetyl-2-amino-6-oxo-1-{4-[(pyrimidin-2-ylamino)sulfonyl]-phenyl}-1,6-dihydropyrimidine-3-carboxylic acid ethyl ester 
• 1100799-32-3 N-{4-[(pyrimidin-2-ylamino)sulfonyl]phenyl}-5-methyl-N,1-diphenyl-1H-pyrazole-4-carbohydrazonamide 
• 1100799-23-2 4-(3,5-diacetyl-6-methyl-2-oxo-2H-pyridin-1-yl)-N-pyrimidin-2-ylbenzene-sulfonamide 
• 1100799-19-6 4-(3-acetyl-6-amino-5-cyano-2-oxo-2H-pyridin-1-yl)-N-pyrimidin-2-ylbenzene-sulfonamide 
• 1100799-20-9 5-acetyl-2-amino-6-oxo-1-{4-[(pyrimidin-2-ylamino)sulfonyl]-phenyl}-1,6-dihydropyrimidine-3-carboxamide 

Relevant articles and documents

β-oxoanilides in heterocyclic synthesis: An expeditious synthesis of new polyfunctionally substituted pyridine and pyrazole derivatives

(Chemical Equation Presented) 3-Oxo-N-{4-[(pyrimidin-2-ylamino)sulfonyl] phenyl}butanamide 3 was condensed with (DMF-DMA) in refluxing dry dioxane to yield branched structure 4 not its linear isomeric 5. Compound 4 readily reacted with active methylene to