Molecular structure of 1-Fluorodecane, CAS Number: 334-56-5
1-Fluorodecane (CAS 334-56-5)
CAS Number:
334-56-5
Molecular Weight:
160.27
Molecular Formula:
F(CH2)9CH3
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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1-Fluorodecane serves as a non-polar solvent in experimental applications. It interacts with other non-polar substances, aiding in the dissolution and separation of various compounds during experimental procedures. At the molecular level, 1-Fluorodecane exhibits a mechanism of action that involves weak intermolecular forces, allowing it to effectively solvate non-polar molecules and facilitate their manipulation in laboratory applications. In experimental applications, 1-Fluorodecane′s mechanism of action involves its ability to effectively dissolve and disperse non-polar substances, contributing to the successful execution of laboratory procedures.
1-Fluorodecane (CAS 334-56-5) References
- Alkylation of magnesium enamide with alkyl chlorides and fluorides. | Hatakeyama, T., et al. 2005. J Am Chem Soc. 127: 14192-3. PMID: 16218607
- Catalytic C-F activation and hydrodefluorination of fluoroalkyl groups. | Meier, G. and Braun, T. 2009. Angew Chem Int Ed Engl. 48: 1546-8. PMID: 19148912
- Hydrodefluorination and other hydrodehalogenation of aliphatic carbon-halogen bonds using silylium catalysis. | Douvris, C., et al. 2010. J Am Chem Soc. 132: 4946-53. PMID: 20218686
- Solvent dependent reductive defluorination of aliphatic C-F bonds employing Sm(HMDS)2. | Janjetovic, M., et al. 2013. Chem Commun (Camb). 49: 1826-8. PMID: 23358653
- Selective C-F bond activation: substitution of unactivated alkyl fluorides using YbI₃. | Träff, AM., et al. 2013. Angew Chem Int Ed Engl. 52: 12073-6. PMID: 24115642
- Mild and selective activation and substitution of strong aliphatic C-F bonds. | Janjetovic, M., et al. 2015. Chemistry. 21: 3772-7. PMID: 25601723
- Artificial Solid Electrolyte Interphase-Protected LixSi Nanoparticles: An Efficient and Stable Prelithiation Reagent for Lithium-Ion Batteries. | Zhao, J., et al. 2015. J Am Chem Soc. 137: 8372-5. PMID: 26091423
- Catalytic Iodination of the Aliphatic C-F Bond by YbI3(THF)3: Mechanistic Insight and Synthetic Utility. | Janjetovic, M., et al. 2016. Org Lett. 18: 2804-7. PMID: 27243465
- Pseudomonas sp. Strain 273 Degrades Fluorinated Alkanes. | Xie, Y., et al. 2020. Environ Sci Technol. 54: 14994-15003. PMID: 33190477
- Pseudomonas sp. Strain 273 Incorporates Organofluorine into the Lipid Bilayer during Growth with Fluorinated Alkanes. | Xie, Y., et al. 2022. Environ Sci Technol. 56: 8155-8166. PMID: 35642897
- Selective determination of organofluorine compounds by capillary column gas chromatography with an atmospheric pressure helium microwave-induced plasma detector | J. H. Brill, B. A. Narayanan, J. P. Doom, J. P. McCormick. 1988. Journal of High Resolution Chromatography. 11: 368-374.
- Regioselective α-alkylation of ketones with alkyl chlorides and fluorides via highly nucleophilic magnesium enamides | Takuji Hatakeyama a, Shingo Ito b, Hiroaki Yamane a, Masaharu Nakamura a, Eiichi Nakamura b. 2007. Tetrahedron. 63: 8440-8448.
- A catalytic CC bond-forming reaction between aliphatic fluorohydrocarbons and arylsilanes | Nicole Lühmann, Robin Panisch, Thomas Müller. 2010. 24: 533-537.
- The guest ordering and dynamics in urea inclusion compounds studied by solid-state 1H and 13C MAS NMR spectroscopy | Xiaorong Yang, Klaus Müller. 2011. Journal of Molecular Structure. 1006: 113-120.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1-Fluorodecane, 1 g | sc-224678 | 1 g | $163.00 |