79044-04-5

Basic information

• Product Name: N-(4-Chloro-2-vinyl-phenyl)-acetamide
• Synonyms: N-(4-Chloro-2-vinyl-phenyl)-acetamide
• CAS NO: 79044-04-5
• Molecular Weight: 195.648
• Mol File: 79044-04-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N-(4-Chloro-2-vinyl-phenyl)-acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-Chloro-2-vinyl-phenyl)-acetamide(79044-04-5)
• EPA Substance Registry System: N-(4-Chloro-2-vinyl-phenyl)-acetamide(79044-04-5)

Safety Data

• Hazardous Substances Data: 79044-04-5(Hazardous Substances Data)

Upstream product

• 74-85-1 ethene 
• 539-03-7 N-(4-chlorophenyl)acetamide 
• 116035-66-6 N-(4-chloro-2-iodophenyl)acetamide 
• 7486-35-3 tri-n-butyl(vinyl)tin 
• 57045-85-9 2-bromo-4-chloroacetanilide 

Downstream Products

• 864749-97-3 N-(4-chloro-2-vinyl-phenyl)-N-(2,5-dibromo-benzyl)-acetamide 
• 1810-72-6 2,6-dichloroquinoline 
• 947689-06-7 C₂₇H₂₇ClNO₆P 

Relevant articles and documents

A new method for the generation of indole-2,3-quinodimethanes and 2-(N-alkoxycarbonylamino)-1,3-dienes. Intramolecular Heck/Diels-Alder cycloaddition cascade starting from acyclic α-phosphono enecarbamates

An intramolecular Heck/Diels-Alder cycloaddition cascade starting from acyclic α-phosphono enecarbamates has been developed to prepare nitrogen heterocycles via indole-2,3-quinodimethanes and 2-(N-alkoxycarbonylamino)-1,3- dienes. The Royal Society of Che

Fused heterotricyclic compounds as inhibitors of 17beta-hydroxysteroid dehydrogenase 3

Fused heterotricyclic compounds, methods of using such compounds in the treatment of hormone sensitive diseases such as prostate cancer, and pharmaceutical compositions containing such compounds.

Ortho Vinylation of Aromatic Amides via Cyclopalladation Complexes

The reaction of acetanilide and meta- and para-substituted acetanilides with palladium acetate has given new ortho-palladated complexes 2a-j, which reacted with carbon monoxide, ethylene, or methyl vinyl ketone to produce the corresponding N-acylanthranilic esters 4a-m, 2-acetaminostyrenes 9k-p, and 4-aryl-3-buten-2-one derivatives 9a-j, respectively.Reactions of 2a with substituted olefins proceeded readily to give the 2-olefins 8a-h.Ortho-substituted acetanilides and N-methylacetanilide did not undergo complex formation with palladium acetate.