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Molecular structure of Bicyclo[3.3.1]nonan-9-one, CAS Number: 17931-55-4
Bicyclo[3.3.1]nonan-9-one (CAS 17931-55-4)
CAS Number:
17931-55-4
Molecular Weight:
138.21
Molecular Formula:
C9H14O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Bicyclo[3.3.1]nonan-9-one, also known as bicyclononane, is a cyclic organic compound. It is a saturated hydrocarbon and a member of the bicycloalkyl family. The compound is known to be a good electron acceptor and acts as a catalyst in certain reactions. In scientific research, it is used as a building block for synthesizing other compounds, such as polymers, fragrances, polycyclic aromatic hydrocarbons, and heterocyclic compounds. In addition, Bicyclo[3.3.1]nonan-9-onee has been used to study the properties of aromatic compounds, the effects of steric hindrance, and the reactivity of organic molecules.
Bicyclo[3.3.1]nonan-9-one (CAS 17931-55-4) References
- Structure Elucidation With Lanthanide Induced Shifts. 9. Bicyclo[3.3.1]Nonan-9-One | Douglas J. Raber, et al. 1980. Tetrahedron Letters. 21: 677-680.
- Carbon-13 Nmr Spectra Of Solid Bicyclo[3. 3. 1]Nonan-9-One. Conformational Studies In The Solid State | Roderick E. Wasylishen and Kenneth J. Friesen. 1980. Organic Magnetic Resonance. 13: 343-344.
- Allylic Geminal Diacetates As A A1,A3 Synthon. A Convenient Synthesis Of Bicyclo[3.3.1]Nonan-9-One Derivatives | Xiyan Lu and Yujin Huang. 1986. Tetrahedron Letters. 27: 1615-1616.
- Polymorphism In Bicyclo[3.3.1]Nonan-9-One: A Molecular Solid That Can Exist In Both Its Ordered And Its Disordered Phases At Room Temperature | Mary Anne White and Allyson Perrott. 1991. Journal of Solid State Chemistry. 90: 87-91.
- The Low-Temperature Structures Of Bicyclo[3.3.1]Nonan-9-One And 3-Azabicyclo[3.2.2]Nonane | . 1999. Zeitschrift für Kristallographie - Crystalline Materials. 214: 480-485.
- Stereoselective Synthesis of Substituted Bicyclo-[3.3.1]-nonan-9-ones by Additions of Enamines of Cyclohexanones to 4-Ethoxy-1,1,1-trifluorobut-3-ene-2-one | Rebecca J Andrew, et al. 2000. Tetrahedron. 56: 7255-7260.
- The Molecular Structure And Conformation Of Bicyclo[3.3.1]Nonan-9-One: Ab Initio And Dft Calculations | Jaebum Choo, et al. 2002. Journal of Molecular Structure: THEOCHEM. 619: 113-120.
- Kappa-Receptor Selective Binding Of Opioid Ligands With A Heterocyclic Bicyclo[3.3.1]Nonan-9-One Structure | S. Benyhe, et al. 2003. Acta Biologica Hungarica. 54: 147–155.
- A Rapid Acquisition Of The Bicyclo[3.3.1]Nonan-9-One Core Present In Garsubellin A And Related Phloroglucins | Goverdhan Mehta and Mrinal K. Bera. 2006. Tetrahedron Letters. 47: 689-692.
- A Concise Approach Towards The Bicyclo[3.3.1]Nonan-9-One Core Present In The Phloroglucin Natural Product Hyperforin | Goverdhan Mehta and Mrinal K. Bera. 2008. Tetrahedron Letters. 49: 1417-1420.
- A Stereodefined Approach Towards The Bicyclo[3.3.1]Nonan-9-One Core Of The Phloroglucin Natural Products Guttiferone A And Hypersampsone F | Goverdhan Mehta, et al. 2008. Tetrahedron Letters. 49: 1121-1124.
- Organocascade Synthesis Of Bicyclo[3.3.1]Nonan-9-Ones Initiated By An Unusual 1,6-Addition Of Cyclohexanones To (E)-2-(3-Arylallylidene)-1h-Indene-1,3(2h)-Diones | De-Chih Wang, et al. 2017. Advanced Synthesis & Catalysis. 359: 3005-3013.
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| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Bicyclo[3.3.1]nonan-9-one, 1 g | sc-227357 | 1 g | $548.00 |