N-Benzyl nortropinone
CAS: 28957-72-4
Ref. 3D-FB18303
| 2g | Discontinued | ||
| 5g | Discontinued | ||
| 10g | Discontinued | ||
| 25g | Discontinued | ||
| 50g | Discontinued |
Product Information
Name:
N-Benzyl nortropinone
Synonyms:
- 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
Description:
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.
Notice:
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Brand:
Biosynth
Long term storage:
Notes:
Chemical properties
Molecular weight:
215.29 g/mol
Formula:
C14H17NO
Purity:
Min. 95%
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HS code:
