Date published: 2025-12-3

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1-Fluoronaphthalene (CAS 321-38-0)

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CAS Number:
321-38-0
Molecular Weight:
146.16
Molecular Formula:
C10H7F
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-Fluoronaphthalene is used in organic chemistry for its applications as a building block in the synthesis of complex organic molecules. It serves as a precursor in the creation of various fluoroaromatic compounds, which are important for studies in material science and electronic device fabrication. 1-Fluoronaphthalene is utilized to explore its incorporation into liquid crystals and conductive polymers, enhancing their properties for better performance in technological applications. Its role in photochemical studies is of interest due to the unique behaviors exhibited by fluorinated aromatics when exposed to light.


1-Fluoronaphthalene (CAS 321-38-0) References

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  2. Characterization of monofluorinated polycyclic aromatic compounds by 1H, 13C and 19F NMR spectroscopy.  |  Lutnaes, BF., et al. 2005. Magn Reson Chem. 43: 588-94. PMID: 15809969
  3. Determination of aromatic sulphur compounds in heavy gas oil by using (low-)flow modulated comprehensive two-dimensional gas chromatography-triple quadrupole mass spectrometry.  |  Franchina, FA., et al. 2015. J Chromatogr A. 1387: 86-94. PMID: 25704775
  4. A Validated RP-HPLC Method for the Analysis of 1-Fluoronaphthalene and Its Process-Related Impurities.  |  Karagiannidou, EG., et al. 2015. J Chromatogr Sci. 53: 1296-302. PMID: 25713107
  5. Direct Arylation of Simple Arenes with Aryl Bromides by Synergistic Silver and Palladium Catalysis.  |  Tlahuext-Aca, A., et al. 2021. ACS Catal. 11: 1430-1434. PMID: 34790433
  6. Radical-anion coupling through reagent design: hydroxylation of aryl halides.  |  Greener, AJ., et al. 2021. Chem Sci. 12: 14641-14646. PMID: 34881017
  7. Automation and Microfluidics for the Efficient, Fast, and Focused Reaction Development of Asymmetric Hydrogenation Catalysis.  |  van Putten, R., et al. 2022. ChemSusChem. 15: e202200333. PMID: 35470567
  8. SulfoxFluor-enabled deoxyazidation of alcohols with NaN3.  |  Guo, J., et al. 2022. Nat Commun. 13: 2752. PMID: 35585073
  9. Additive-Induced Vertical Component Distribution Enables High-Performance Sequentially Cast Organic Solar Cells.  |  Li, X., et al. 2022. ACS Appl Mater Interfaces. 14: 25842-25850. PMID: 35635178
  10. Electrochemical Benzylic C(sp3)-H Acyloxylation.  |  Atkins, AP., et al. 2022. Org Lett. 24: 5105-5108. PMID: 35829756
  11. Fibrillization of Non-Fullerene Acceptors Enables 19% Efficiency Pseudo-Bulk Heterojunction Organic Solar Cells.  |  Li, D., et al. 2023. Adv Mater. 35: e2208211. PMID: 36418914
  12. Accessing Unusual Reactivity through Chelation-Promoted Bond Weakening.  |  Boekell, NG., et al. 2023. Inorg Chem. 62: 5040-5045. PMID: 36912617
  13. Unlocking the Nucleophilicity of Strong Alkyl C-H Bonds via Cu/Cr Catalysis.  |  Peng, P., et al. 2023. ACS Cent Sci. 9: 756-762. PMID: 37122460
  14. Effects of a fluoro substituent on the fungal metabolism of 1-fluoronaphthalene.  |  Cerniglia, CE., et al. 1984. Appl Environ Microbiol. 48: 294-300. PMID: 6486779

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1-Fluoronaphthalene, 5 g

sc-237556
5 g
$31.00