Similiar Molecules

• SMILES String: C1CC2CCC1CNC2
• Also know as: 3-azabicyclo[3.2.2]nonane
• InChI=1/C8H15N/c1-2-8-4-3-7(1)5-9-6-8/h7-9H,1-6H2
• Molecular Formula: C8H15N
Reactions where this compound is a reactant:
• (Amide Formation from an Acid Chloride)
0
with 2-chloroacetyl chloride3-azabicyclo[3.2.2]no to form 1-(3-azabicyclo[3.2.2]nonan-3-yl)-2-chloro-ethanone

• with 2-iodoacetyl chloride3-azabicyclo[3.2.2]no to form 1-(3-azabicyclo[3.2.2]nonan-3-yl)-2-iodo-ethanone
  
• with 2,2-dichloroacetyl chloride3-azabicyclo[3.2.2]no to form 1-(3-azabicyclo[3.2.2]nonan-3-yl)-2,2-dichloro-ethanone
  
• with 3H-imidazole-4-carbonyl chloride3-azabicyclo[3.2.2]no to form 3-azabicyclo[3.2.2]nonan-3-yl-(3H-imidazol-4-yl)methanone
  
• with prop-2-enoyl chloride3-azabicyclo[3.2.2]no to form 1-(3-azabicyclo[3.2.2]nonan-3-yl)prop-2-en-1-one
  
• with formyl chloride3-azabicyclo[3.2.2]no to form 3-azabicyclo[3.2.2]nonane-3-carbaldehyde
  
• with chloromethanethioic S-acid3-azabicyclo[3.2.2]no to form 3-azabicyclo[3.2.2]nonane-3-carbothioic S-acid
  
• with S-ethyl chloromethanethioate3-azabicyclo[3.2.2]no to form S-ethyl 3-azabicyclo[3.2.2]nonane-3-carbothioate
  
• with 2-bromoacetyl chloride3-azabicyclo[3.2.2]no to form 1-(3-azabicyclo[3.2.2]nonan-3-yl)-2-bromo-ethanone
  
• with 4-hydroxybutanoyl chloride3-azabicyclo[3.2.2]no to form 1-(3-azabicyclo[3.2.2]nonan-3-yl)-4-hydroxy-butan-1-one
  
• (Nucleophilic Acylation)
0
with 2-chloroacetyl bromide3-azabicyclo[3.2.2]no to form 1-(3-azabicyclo[3.2.2]nonan-3-yl)-2-chloro-ethanone

• with 2-chloroacetyl chloride3-azabicyclo[3.2.2]no to form 1-(3-azabicyclo[3.2.2]nonan-3-yl)-2-chloro-ethanone
  
• with 2-chloroacetyl fluoride3-azabicyclo[3.2.2]no to form 1-(3-azabicyclo[3.2.2]nonan-3-yl)-2-chloro-ethanone
  
• with 2-chloroacetyl iodide3-azabicyclo[3.2.2]no to form 1-(3-azabicyclo[3.2.2]nonan-3-yl)-2-chloro-ethanone
  
• with 2-iodoacetyl bromide3-azabicyclo[3.2.2]no to form 1-(3-azabicyclo[3.2.2]nonan-3-yl)-2-iodo-ethanone
  
• with 2-iodoacetyl chloride3-azabicyclo[3.2.2]no to form 1-(3-azabicyclo[3.2.2]nonan-3-yl)-2-iodo-ethanone
  
• with 2-iodoacetyl fluoride3-azabicyclo[3.2.2]no to form 1-(3-azabicyclo[3.2.2]nonan-3-yl)-2-iodo-ethanone
  
• with 2-iodoacetyl iodide3-azabicyclo[3.2.2]no to form 1-(3-azabicyclo[3.2.2]nonan-3-yl)-2-iodo-ethanone
  
• with 2,2-dichloroacetyl bromide3-azabicyclo[3.2.2]no to form 1-(3-azabicyclo[3.2.2]nonan-3-yl)-2,2-dichloro-ethanone
  
• with 2,2-dichloroacetyl chloride3-azabicyclo[3.2.2]no to form 1-(3-azabicyclo[3.2.2]nonan-3-yl)-2,2-dichloro-ethanone
  
See all 29 reactions
• (Sn2)
0
with bromomethane3-azabicyclo[3.2.2]no to form 3-methyl-3-azabicyclo[3.2.2]nonane

• with chloromethane3-azabicyclo[3.2.2]no to form 3-methyl-3-azabicyclo[3.2.2]nonane
  
• with fluoromethane3-azabicyclo[3.2.2]no to form 3-methyl-3-azabicyclo[3.2.2]nonane
  
• with iodomethane3-azabicyclo[3.2.2]no to form 3-methyl-3-azabicyclo[3.2.2]nonane
  
• with 2-bromoacetonitrile3-azabicyclo[3.2.2]no to form 2-(3-azabicyclo[3.2.2]nonan-3-yl)acetonitrile
  
• with 2-chloroacetonitrile3-azabicyclo[3.2.2]no to form 2-(3-azabicyclo[3.2.2]nonan-3-yl)acetonitrile
  
• with 2-fluoroacetonitrile3-azabicyclo[3.2.2]no to form 2-(3-azabicyclo[3.2.2]nonan-3-yl)acetonitrile
  
• with 2-iodoacetonitrile3-azabicyclo[3.2.2]no to form 2-(3-azabicyclo[3.2.2]nonan-3-yl)acetonitrile
  
• with 1-bromo-2-chloro-ethane3-azabicyclo[3.2.2]no to form 3-(2-chloroethyl)-3-azabicyclo[3.2.2]nonane
  
• with 1,2-dichloroethane3-azabicyclo[3.2.2]no to form 3-(2-chloroethyl)-3-azabicyclo[3.2.2]nonane
  
See all 65 reactions
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