39778-79-5

Basic information

• Product Name: cis-octahydro-1-methyl-3a-phenylindol-2-one
• CAS NO: 39778-79-5
• Molecular Weight: 229.322
• Mol File: 39778-79-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: cis-octahydro-1-methyl-3a-phenylindol-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: cis-octahydro-1-methyl-3a-phenylindol-2-one(39778-79-5)
• EPA Substance Registry System: cis-octahydro-1-methyl-3a-phenylindol-2-one(39778-79-5)

Safety Data

• Hazardous Substances Data: 39778-79-5(Hazardous Substances Data)

Upstream product

• 129920-35-0 2,2-Dichloro-N-((1R,2S)-2-hydroxy-2-phenyl-cyclohexyl)-N-methyl-acetamide 
• 129920-34-9 (1R^*,2S^*)-2-(methylamino)-1-phenylcyclohexane-1-ol 
• 771-98-2 1-Phenylcyclohexene 
• 5775-23-5 1-phenylcyclohexene oxide 
• 39778-70-6 1-phenyl-cis-bicyclo<4.2.0>octan-7-one 
• 256506-05-5 N-methyl-N-(2-phenyl-2-cyclohex-1-yl)trichloroacetamide 
• 39778-86-4 C₁₅H₁₉NO 
• 125032-11-3 α,α-dichloro-N-methyl-N-(2-phenylcyclohex-2-en-1-yl)-acetamide 

Downstream Products

• 35119-24-5 1-methyl-3a-phenyl-cis-octahydroindole 

Relevant articles and documents

Radical Cyclization of N-(Cyclohex-2-enyl)-α,α-dichloroacetamides. Stereoselective Syntheses of (+/-)-Mesembranol and (+/-)-Elwesine

Stereoselective syntheses of the Sceletium alkaloid (+/-)-mesembranol (2) and the Amaryllidaceae alkaloid (+/-)-elwesine (3) have been achieved.A key step in the syntheses involves the Bu3SnH-mediated radical cyclization of the dichloroacetamides 34 and 4

Stereoselective Preparation of Bicyclic Lactams by Copper- or Ruthenium-catalysed Cyclization of N-Allyltrichloroacetamides: A Novel Entry to Pyrrolidine Alkaloid Skeletons

Cyclization of certain N-allyltrichloroacetamides provides a stereoselective preparative method for several bicyclic lactams.