Cas no 1978-60-5 (Pyridine,4-(3-fluorophenyl)-1,2,3,6-tetrahydro-)

Pyridine,4-(3-fluorophenyl)-1,2,3,6-tetrahydro- is a fluorinated heterocyclic compound featuring a pyridine core substituted with a 3-fluorophenyl group and a partially saturated 1,2,3,6-tetrahydropyridine ring. This structure imparts unique electronic and steric properties, making it a valuable intermediate in pharmaceutical and agrochemical synthesis. The fluorine substituent enhances metabolic stability and bioavailability, while the tetrahydropyridine moiety offers versatility in further functionalization. Its well-defined reactivity profile allows for selective modifications, facilitating the development of bioactive molecules. The compound is typically handled under inert conditions due to its sensitivity to oxidation. High-purity grades are available for research and industrial applications requiring precise structural control.
Pyridine,4-(3-fluorophenyl)-1,2,3,6-tetrahydro- structure
1978-60-5 structure
Product Name:Pyridine,4-(3-fluorophenyl)-1,2,3,6-tetrahydro-
CAS No:1978-60-5
MF:C11H12FN
MW:177.218086242676
CID:118260
PubChem ID:11389726
Update Time:2025-11-02

Pyridine,4-(3-fluorophenyl)-1,2,3,6-tetrahydro- Chemical and Physical Properties

Names and Identifiers

    • Pyridine,4-(3-fluorophenyl)-1,2,3,6-tetrahydro-
    • 4-(3-FLUOROPHENYL)-1,2,3,6-TETRAHYDROPYRIDINE
    • 4-(3-Fluoro-phenyl)-1,2,3,6-tetrahydro-pyridine
    • 4-(3-Fluor-phenyl)-1,2,3,6-tetrahydro-pyridin
    • 4-< 3-Fluor-phenyl> -1,2,3,6-tetrahydro-pyridin
    • AG-E-44542
    • AGN-PC-0084YN
    • AmbkkkkK546
    • CTK4E2324
    • SureCN4789465
    • ILCNYFXNNQYRJP-UHFFFAOYSA-N
    • DTXSID00464320
    • EN300-53371
    • 1978-60-5
    • AKOS000205266
    • CS-0304463
    • SCHEMBL4789465
    • Inchi: 1S/C11H12FN/c12-11-3-1-2-10(8-11)9-4-6-13-7-5-9/h1-4,8,13H,5-7H2
    • InChI Key: ILCNYFXNNQYRJP-UHFFFAOYSA-N
    • SMILES: FC1=CC=CC(=C1)C1=CCNCC1

Computed Properties

  • Exact Mass: 177.09546
  • Monoisotopic Mass: 177.095377549g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 1
  • Complexity: 200
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.4
  • Topological Polar Surface Area: 12?2

Experimental Properties

  • PSA: 12.03
  • LogP: 2.53120

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Additional information on Pyridine,4-(3-fluorophenyl)-1,2,3,6-tetrahydro-

Comprehensive Guide to Pyridine,4-(3-fluorophenyl)-1,2,3,6-tetrahydro- (CAS No. 1978-60-5): Properties, Applications, and Market Insights

Pyridine,4-(3-fluorophenyl)-1,2,3,6-tetrahydro- (CAS No. 1978-60-5) is a fluorinated pyridine derivative that has garnered significant attention in pharmaceutical and agrochemical research. This compound belongs to the class of heterocyclic organic compounds, which are widely used as building blocks in drug discovery and material science. The presence of both pyridine and fluorophenyl moieties in its structure makes it a versatile intermediate for synthesizing bioactive molecules.

The chemical structure of Pyridine,4-(3-fluorophenyl)-1,2,3,6-tetrahydro- features a partially hydrogenated pyridine ring attached to a 3-fluorophenyl group. This unique combination enhances its reactivity and binding affinity, making it valuable for designing central nervous system (CNS) targeting drugs. Researchers have explored its potential in developing novel neurological therapeutics, particularly for conditions like Parkinson's disease and epilepsy, which aligns with current trends in precision medicine.

In recent years, the demand for fluorinated pyridine derivatives has surged due to their improved metabolic stability and membrane permeability compared to non-fluorinated analogs. This compound's lipophilicity and electron-withdrawing properties, imparted by the fluorine atom, make it particularly useful in medicinal chemistry optimization. Pharmaceutical companies are increasingly incorporating such fluorinated building blocks to enhance drug candidates' bioavailability and target selectivity.

The synthesis of Pyridine,4-(3-fluorophenyl)-1,2,3,6-tetrahydro- typically involves catalytic hydrogenation of corresponding pyridine precursors followed by fluorophenyl group introduction. Advanced green chemistry approaches are being developed to improve the yield and reduce environmental impact, responding to the growing industry focus on sustainable synthesis methods. These innovations address common search queries about eco-friendly chemical production and atom economy in organic synthesis.

Beyond pharmaceuticals, this compound shows promise in agrochemical applications. Its structural features can be leveraged to develop new-generation crop protection agents with improved efficacy and reduced environmental persistence. The fluorine atom in the molecule often enhances pesticidal activity while maintaining favorable toxicological profiles, a key consideration in modern sustainable agriculture practices.

Market analysis indicates steady growth in demand for specialty fluorinated compounds like Pyridine,4-(3-fluorophenyl)-1,2,3,6-tetrahydro-. The global market is driven by increasing R&D investments in targeted drug discovery and the need for advanced crop science solutions. Quality standards for this compound typically require high purity levels (>98%), with rigorous HPLC analysis and spectroscopic characterization (including NMR and mass spectrometry) to ensure batch consistency.

Storage and handling of Pyridine,4-(3-fluorophenyl)-1,2,3,6-tetrahydro- require standard laboratory precautions for organic compounds. It should be kept in airtight containers under inert atmosphere to prevent degradation, with recommended storage temperatures between 2-8°C for long-term stability. These handling protocols address frequently searched questions about chemical storage best practices and compound stability considerations.

Recent scientific literature highlights innovative applications of this compound in material science, particularly in developing organic electronic materials. The conjugated system in its structure makes it potentially useful for creating semiconducting polymers or light-emitting materials, aligning with the booming interest in flexible electronics and OLED technologies.

For researchers working with Pyridine,4-(3-fluorophenyl)-1,2,3,6-tetrahydro-, proper analytical characterization is crucial. Standard protocols involve chromatographic purity assessment and structural confirmation through FT-IR spectroscopy and elemental analysis. These quality control measures respond to common search terms about compound verification methods in chemical research.

The future outlook for Pyridine,4-(3-fluorophenyl)-1,2,3,6-tetrahydro- appears promising, with potential expansions into diagnostic imaging agents and therapeutic radiopharmaceuticals. The fluorine atom's presence makes it particularly interesting for PET tracer development, tapping into the growing field of molecular imaging. This application potential addresses trending searches about next-generation diagnostic tools in modern healthcare.

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