Cas no 313993-81-6 (4-3-(4-fluorophenyl)propylpiperidine)

4-3-(4-Fluorophenyl)propylpiperidine is a fluorinated piperidine derivative with potential applications in pharmaceutical and organic synthesis. Its structure, featuring a 4-fluorophenylpropyl side chain, enhances its utility as an intermediate in the development of bioactive compounds, particularly those targeting central nervous system (CNS) receptors. The fluorine substitution improves metabolic stability and binding affinity, making it valuable for medicinal chemistry research. This compound exhibits favorable physicochemical properties, including moderate lipophilicity, which aids in solubility and bioavailability optimization. Its synthetic versatility allows for further functionalization, enabling the exploration of structure-activity relationships in drug discovery. Suitable for controlled laboratory use, it is typically handled under inert conditions to preserve stability.
4-3-(4-fluorophenyl)propylpiperidine structure
313993-81-6 structure
Product Name:4-3-(4-fluorophenyl)propylpiperidine
CAS No:313993-81-6
MF:C14H20FN
MW:221.313707351685
CID:1447125
PubChem ID:3059022
Update Time:2025-06-14

4-3-(4-fluorophenyl)propylpiperidine Chemical and Physical Properties

Names and Identifiers

    • Piperidine, 4-[3-(4-fluorophenyl)propyl]-
    • 4-3-(4-fluorophenyl)propylpiperidine
    • NOAWTCRBYKDFGP-UHFFFAOYSA-N
    • 4-[3-(4-fluorophenyl)propyl]piperidine
    • 4-(3-(4-fluorophenyl)propyl)-piperidine
    • EN300-1866357
    • 313993-81-6
    • SCHEMBL4319526
    • 4-[3-(4-fluorophenyl)1-propyl]piperidine
    • 4-(3-(4-fluorophenyl)propyl)piperidine
    • Inchi: 1S/C14H20FN/c15-14-6-4-12(5-7-14)2-1-3-13-8-10-16-11-9-13/h4-7,13,16H,1-3,8-11H2
    • InChI Key: NOAWTCRBYKDFGP-UHFFFAOYSA-N
    • SMILES: FC1C=CC(=CC=1)CCCC1CCNCC1

Computed Properties

  • Exact Mass: 221.1581
  • Monoisotopic Mass: 221.157977804g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 4
  • Complexity: 181
  • 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: 3.7
  • Topological Polar Surface Area: 12?2

Experimental Properties

  • PSA: 12.03

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Additional information on 4-3-(4-fluorophenyl)propylpiperidine

Comprehensive Overview of 4-3-(4-fluorophenyl)propylpiperidine (CAS No. 313993-81-6): Properties, Applications, and Research Insights

4-3-(4-fluorophenyl)propylpiperidine (CAS No. 313993-81-6) is a specialized organic compound that has garnered significant attention in pharmaceutical and chemical research due to its unique structural features and potential applications. The compound belongs to the piperidine derivative family, characterized by a fluorophenyl group attached to a propyl chain, which enhances its reactivity and binding affinity in biological systems. Researchers and industry professionals often search for terms like "4-3-(4-fluorophenyl)propylpiperidine synthesis," "CAS 313993-81-6 applications," and "fluorophenyl piperidine derivatives" to explore its utility in drug discovery and material science.

The molecular structure of 4-3-(4-fluorophenyl)propylpiperidine incorporates a piperidine ring, a common motif in medicinal chemistry, known for its role in modulating central nervous system (CNS) activity. The addition of a 4-fluorophenyl group introduces electron-withdrawing properties, which can influence the compound's pharmacokinetics and metabolic stability. This structural combination makes it a candidate for investigating neurotransmitter receptor interactions, a hot topic in neuroscience and psychiatric drug development. Recent studies have linked similar compounds to potential applications in addressing neurodegenerative disorders, aligning with growing public interest in mental health and cognitive wellness.

From a synthetic chemistry perspective, CAS No. 313993-81-6 is often discussed in the context of heterocyclic compound optimization. Its synthesis typically involves multi-step reactions, including alkylation and aromatic substitution, to achieve high purity and yield. Laboratories focusing on high-throughput screening or fragment-based drug design may prioritize this compound due to its modular structure, which allows for further derivatization. Searches for "piperidine-based scaffold design" or "fluorinated aromatic compounds in drug discovery" reflect the broader scientific community's interest in these areas.

In addition to pharmaceutical applications, 4-3-(4-fluorophenyl)propylpiperidine has potential uses in material science, particularly in the development of advanced polymers and liquid crystals. The fluorophenyl moiety can enhance thermal stability and optical properties, making it relevant for industries exploring next-generation electronic displays or high-performance coatings. This interdisciplinary appeal has led to increased demand for technical data sheets and safety profiles of CAS 313993-81-6, especially among R&D teams working on sustainable materials.

Environmental and regulatory considerations are also critical when handling 4-3-(4-fluorophenyl)propylpiperidine. While not classified as hazardous under standard guidelines, proper storage conditions (e.g., inert atmosphere, low temperature) are recommended to maintain its stability. Researchers frequently inquire about "green chemistry alternatives for piperidine derivatives" or "biodegradability of fluorinated compounds," highlighting the shift toward eco-friendly synthetic routes. These trends align with global initiatives like the UN Sustainable Development Goals (SDGs), particularly those targeting responsible consumption and industrial innovation.

Future research directions for CAS No. 313993-81-6 may focus on its role in precision medicine and targeted therapy, leveraging its structural versatility to address unmet medical needs. Collaborative efforts between academia and industry could accelerate the discovery of novel analogs with improved efficacy and safety profiles. As interest in personalized healthcare grows, compounds like 4-3-(4-fluorophenyl)propylpiperidine will remain at the forefront of scientific exploration, bridging gaps between chemical innovation and therapeutic advancement.

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