111733-88-1

Basic information

• Product Name: Ethanone, 2-(hexahydro-1H-azepin-1-yl)-1-phenyl-
• CAS NO: 111733-88-1
• Molecular Formula: C14H19NO
• Molecular Weight: 217.311
• Mol File: 111733-88-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Ethanone, 2-(hexahydro-1H-azepin-1-yl)-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 2-(hexahydro-1H-azepin-1-yl)-1-phenyl-(111733-88-1)
• EPA Substance Registry System: Ethanone, 2-(hexahydro-1H-azepin-1-yl)-1-phenyl-(111733-88-1)

Safety Data

• Hazardous Substances Data: 111733-88-1(Hazardous Substances Data)

Upstream product

• 111-49-9 hexamethylene imine 
• 70-11-1 α-bromoacetophenone 
• 532-27-4 1-chloroacetophenone 

Downstream Products

• 21053-50-9 N-(β-phenethyl)-perhydroazepin-2-one 
• 474104-27-3 (S)-(+)-2-(hexahydroazepin-1-yl)-1-phenylethanol 
• 155783-52-1 (R)-(-)-2-(hexahydroazepin-1-yl)-1-phenylethanol 

Relevant articles and documents

Boranes in Synthesis. 2. Asymmetric Synthesis of β-Amino Alcohols. A Facile Conversion of 2-Amino Acetophenones to the Corresponding β-Amino Alcohols in High Enantiomeric Purity

The asymmetric reduction of 2-amino acetophenones with Ipc2BH or Ipc2BCl at -78 deg C, yields the corresponding β-amino alcohols in good to excellent yields.Although only modest (12-45percent ee) enantiomeric excesses were obtained with Ipc2BH, 75-99perce

Regioselective synthesis of piperidinones by metal catalyzed ring expansion-carbonylation reactions. Remarkable cobalt and/or ruthenium carbonyl catalyzed rearrangement and cyclization reactions

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