N-Benzyl nortropinone
CAS: 28957-72-4
Ref. 3D-FB18303
| 2g | To inquire | ||
| 5g | To inquire | ||
| 10g | To inquire | ||
| 25g | To inquire | ||
| 50g | To inquire |
Product Information
- 8-Aza-8-benzylbicyclo[3,2,1]octan-3-one8-Benzylnortropan-3-one8-Benzyl-1a-H,5a-H-nortropan-3-one
- 1αH,5αH-Tropan-3-one, 9-phenyl-
- 3-Benzyl-3,8-Diazabicyclo[3.2.1]Octane
- 3-Benzyl-3-Azedicyclo(3,2,1)Octan-8-One
- 3-Nortropanone, 8-benzyl-
- 8-(Phenylmethyl)-8-azabicyclo[3.2.1]octan-3-one
- 8-Aza-8-Benzylbicyclo[3,2,1]Octan-3-One
- 8-Aza-8-benzylbicyclo[3,2,1]octan-3-one,8-Benzylnortropan-3-one
- 8-Azabicyclo[3.2.1]octan-3-one, 8-(phenylmethyl)-
- 8-Benzyl-1αH,5αH-nortropan-3-one
- See more synonyms
- 8-Benzyl-3-nortropanone
- 8-Benzyl-8-Azabicyclo[3.2.1]Octan-3-One
- 8-Benzylbicyclo[3.2.1]octan-3-one
- 8-Benzylnortropan-3-One
- 8-Benzyltropinone
- N-Benzyl-3-tropinone
- N-Benzylnortropinone
- N-benzyl-Nortropinone
N-Benzyl nortropinone is a diastereomer that was synthesized using immobilization techniques. It has been shown to have nucleophilic and activated functionalities, which makes it suitable for use in synthetic reactions. N-Benzyl nortropinone can be used as a linker between amines and chloride. The synthesis of this compound involves the reaction of chloroacetonitrile with anhydrous ammonia and triethylamine in the presence of ammonium nitrate. This method is advantageous because it does not require the use of organic solvents, such as trifluoroacetic acid or hydroxyl group.
Chemical properties
Technical inquiry about: 3D-FB18303 N-Benzyl nortropinone
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