117194-86-2

Basic information

• Product Name: (E)-3-(2-tert-Butylsulfanyl-phenyl)-2-cyano-N-(2-morpholin-4-yl-ethyl)-acrylamide
• Synonyms: (E)-3-(2-tert-Butylsulfanyl-phenyl)-2-cyano-N-(2-morpholin-4-yl-ethyl)-acrylamide
• CAS NO: 117194-86-2
• Molecular Weight: 373.519
• Mol File: 117194-86-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (E)-3-(2-tert-Butylsulfanyl-phenyl)-2-cyano-N-(2-morpholin-4-yl-ethyl)-acrylamide(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-3-(2-tert-Butylsulfanyl-phenyl)-2-cyano-N-(2-morpholin-4-yl-ethyl)-acrylamide(117194-86-2)
• EPA Substance Registry System: (E)-3-(2-tert-Butylsulfanyl-phenyl)-2-cyano-N-(2-morpholin-4-yl-ethyl)-acrylamide(117194-86-2)

Safety Data

• Hazardous Substances Data: 117194-86-2(Hazardous Substances Data)

Upstream product

• 2038-03-1 4-(2-AMINOETHYL)MORPHOLINE 
• 15029-26-2 2-cyano-N-(2-morpholinoethyl)acetamide 
• 65924-65-4 2-(tert-butylthio)benzaldehyde 

Relevant articles and documents

Sur le mecanisme de la Reaction de Meth-Cohn-Tarnowski de preparation des thiocoumarines

Reaction of 2-t-butylthiobenzaldehyde with N-(2-dialkylaminoethyl)-cyanacetamides followed by heating of the resulting 3-(2-t-butylthiophenyl)-2-cyanoacrylamides in polyphosphoric acid leads to the formation of 3-carboxamido-2-imino-2H-benzothiopyrane intermediates which afford thiocoumarins on hydrolysis.The authors postulate the intermediate formation of a thiophenate ion by an electronic mechanism involving six centers.