| Weight | 153.225 g/mol |
|---|---|
| Formula | C9H15NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
9-Methyl-9-azabicyclo[3.3.1]nonan-3-one (552-70-5)
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- Sigma-Aldrich - Search for 9-Methyl-9-azabicyclo[3.3.1]nonan-3-one
- Fisher Scientific - Search for 9-Methyl-9-azabicyclo[3.3.1]nonan-3-one
- TCI - Search for 9-Methyl-9-azabicyclo[3.3.1]nonan-3-one
- Assymetric syntheses of the ladybug alkaloid adaline and 1-methyl-9-azabicyclo [3.3.1]nonan-3-one (Tetrahedron, 1982)
- Heterocyclization of tropinone oximes and 3-methyl-3-azabicyclo[3.3.1.]-nonan-9-one with acetylene in a superbasic medium (Chemistry of Heterocyclic Compounds, 1999)
- Incipient nucleophilic additions. III. 3-Oxa-9-methyl-9-azabicyclo[3,3,1]nonan-7-one (Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry, 1975)
- Synthesis, structural and conformational study of 3-methyl-3-azabicyclo[3.2.1]octan-8-one and 3-methyl-3-azabicyclo[3.3.1]nonan-9-one oximes (Journal of Molecular Structure, 2003)
- 2,4-Bis(2-fluorophenyl)-1-methyl-3-azabicyclo[3.3.1]nonan-9-one (Acta Crystallographica Section E-structure Reports Online, 2010)
- 2,4-Bis(2-ethoxyphenyl)-7-methyl-3-azabicyclo[3.3.1]nonan-9-one (Acta Crystallographica Section E-structure Reports Online, 2011)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCN1C2CCCC1CC(=O)C2
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InChIKeyRHWSKVCZXBAWLZ-UHFFFAOYSA-N
- Pubchem - 9-Methyl-9-azabicyclo[3.3.1]nonan-3-one
- Wikipedia - Pseudopelletierine
Pseudopelletierine is the main alkaloid derived from the root-bark of the pomegranate tree (Punica granatum), along with at least three other alkaloids: pelletierine, isopelletierine, and methylpelleteirine (C9H17ON), which yield 1.8, 0.52, 0.01, and 0.20 grams per kilogram of raw bark. Isopelletierine is optically inactive. It is a homolog of tropinone, and can be synthesized in a manner analogous to the classical Robinson tropinone synthesis, using glutaraldehyde (rather than succinaldehyde), acetonedicarboxylic acid, and methylammonium chloride.
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