209742-39-2

Basic information

• Product Name: 3-methylene-2-phenethyl-2,3-dihydroisoindol-1-one
• Synonyms: 3-methylene-2-phenethyl-2,3-dihydroisoindol-1-one
• CAS NO: 209742-39-2
• Molecular Weight: 249.312
• Mol File: 209742-39-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-methylene-2-phenethyl-2,3-dihydroisoindol-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-methylene-2-phenethyl-2,3-dihydroisoindol-1-one(209742-39-2)
• EPA Substance Registry System: 3-methylene-2-phenethyl-2,3-dihydroisoindol-1-one(209742-39-2)

Safety Data

• Hazardous Substances Data: 209742-39-2(Hazardous Substances Data)

Upstream product

• 577-56-0 2-acetyl-benzoic acid 
• 64-04-0 phenethylamine 
• 16727-00-7 potassium 2-acetylbenzoate 
• 1077-79-8 methyl 2-acetylbenzoate 
• 201230-82-2 carbon monoxide 
• 2142-69-0 2-bromophenyl methyl ketone 
• 209742-36-9 2-acetylbenzoic acid methyl ester dimethylketal 
• 33578-00-6 (2-ethynyl)benzoic acid 

Relevant articles and documents

Palladium-catalysed convenient synthesis of 3-methyleneisoindolin-1-ones

2′-Bromoacetophenone reacts with an array of aliphatic primary amines under carbon monoxide pressure in the presence of a catalytic amount of a palladium catalyst to afford 3-methyleneisoindolin-1-ones in moderate yields.

Intramolecular Arylation of Tertiary Enamides through Pd(OAc)2-Catalyzed Dehydrogenative Cross-Coupling Reaction: Construction of Fused N-Heterocyclic Scaffolds and Synthesis of Isoindolobenzazepine Alkaloids

Pd(OAc)2-catalyzed intramolecular dehydrogenative cross-coupling reaction between tertiary enamides, which were derived from the condensation of 2-arylethylamines and methyl o-acetylbenzoate, and arenes enabled synthesis of 7,8-dihydro-5H-benzo