Cas no 2110-18-1 (2-(3-Phenylpropyl)Pyridine)

2-(3-Phenylpropyl)Pyridine is a versatile organic compound featuring a pyridine ring linked to a phenylpropyl side chain. This structure imparts unique reactivity and solubility properties, making it valuable in pharmaceutical and agrochemical synthesis. Its aromatic and heterocyclic characteristics enable applications as an intermediate in the development of bioactive molecules, including potential drug candidates. The compound exhibits moderate polarity, facilitating its use in various organic reactions, such as alkylations and condensations. Its stability under standard conditions ensures reliable handling and storage. Researchers favor 2-(3-Phenylpropyl)Pyridine for its balanced lipophilicity and functional group compatibility, supporting diverse synthetic pathways in medicinal and industrial chemistry.
2-(3-Phenylpropyl)Pyridine structure
2-(3-Phenylpropyl)Pyridine structure
Product Name:2-(3-Phenylpropyl)Pyridine
CAS No:2110-18-1
MF:C14H15N
MW:197.275603532791
MDL:MFCD00191237
CID:84126
PubChem ID:87575415
Update Time:2026-05-14

2-(3-Phenylpropyl)Pyridine Chemical and Physical Properties

Names and Identifiers

    • 2-(3-phenylpropyl)pyridine
    • 2-phenylpropylpyridine
    • UNII-9F0BFM744F
    • Pyridine, 2-(3-phenylpropyl)-
    • alpha-(3-Phenylpropyl)pyridine
    • 9F0BFM744F
    • JJJPNTQYUJPWGQ-UHFFFAOYSA-N
    • cortex pyridine
    • phenylpropylpyridine
    • 3-phenylpropyl pyridine
    • DSSTox_CID_22356
    • DSSTox_RID_80004
    • DSSTox_GSID_42356
    • 2-(3-phenylpropyl)-pyridine
    • FEMA No. 3751
    • 2-(3-cyclohexylpropyl)pyridine
    • 1-Phenyl-3-(2-pyridyl)propane
    • FEMA 3751
    • To
    • 2-(3-Phenylpropyl)Pyridine
    • MDL: MFCD00191237
    • Inchi: 1S/C14H15N/c1-2-7-13(8-3-1)9-6-11-14-10-4-5-12-15-14/h1-5,7-8,10,12H,6,9,11H2
    • InChI Key: JJJPNTQYUJPWGQ-UHFFFAOYSA-N
    • SMILES: N1=C([H])C([H])=C([H])C([H])=C1C([H])([H])C([H])([H])C([H])([H])C1C([H])=C([H])C([H])=C([H])C=1[H]

Computed Properties

  • Exact Mass: 197.12000
  • Monoisotopic Mass: 197.12
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 4
  • Complexity: 161
  • 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
  • Surface Charge: 0
  • Tautomer Count: 2
  • XLogP3: 3.2
  • Topological Polar Surface Area: 12.9

Experimental Properties

  • Color/Form: liquid
  • Density: 1.015?g/mL?at 25?°C(lit.)
  • Boiling Point: 171°C/16mmHg(lit.)
  • Flash Point: Fahrenheit: 212 ° f
    Celsius: 100 ° c
  • Refractive Index: n20/D 1.56(lit.)
  • PSA: 12.89000
  • LogP: 3.25690
  • Solubility: Not determined
  • FEMA: 3751 | 2-(3-PHENYLPROPYL)PYRIDINE

2-(3-Phenylpropyl)Pyridine Security Information

2-(3-Phenylpropyl)Pyridine Customs Data

  • HS CODE:2933399090
  • Customs Data:

    China Customs Code:

    2933399090

    Overview:

    2933399090. Other compounds with non fused pyridine rings in structure. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

2-(3-Phenylpropyl)Pyridine Pricemore >>

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2-(3-Phenylpropyl)Pyridine Related Literature

Additional information on 2-(3-Phenylpropyl)Pyridine

Introduction to 2-(3-Phenylpropyl)Pyridine (CAS No. 2110-18-1)

2-(3-Phenylpropyl)Pyridine, identified by the Chemical Abstracts Service registry number 2110-18-1, is a significant organic compound that has garnered attention in the field of pharmaceutical and chemical research. This compound belongs to the pyridine class, characterized by a six-membered aromatic ring containing a nitrogen atom. The presence of a phenylpropyl side chain further enhances its structural complexity and potential for diverse applications.

The molecular structure of 2-(3-Phenylpropyl)Pyridine consists of a pyridine core substituted with a 3-phenylpropyl group. This configuration imparts unique electronic and steric properties, making it a valuable intermediate in the synthesis of more complex molecules. The compound’s solubility profile, thermal stability, and reactivity are key factors that contribute to its utility in various chemical processes.

In recent years, 2-(3-Phenylpropyl)Pyridine has been extensively studied for its potential applications in medicinal chemistry. Researchers have explored its role as a building block in the development of novel therapeutic agents. The pyridine moiety is particularly noteworthy, as it is a common pharmacophore in many bioactive molecules. Its ability to interact with biological targets makes it an attractive scaffold for drug design.

One of the most compelling areas of research involving 2-(3-Phenylpropyl)Pyridine is its application in the synthesis of small-molecule inhibitors targeting neurological disorders. Studies have demonstrated that derivatives of this compound exhibit promising activity against enzymes and receptors involved in conditions such as Alzheimer’s disease and Parkinson’s disease. The phenylpropyl group contributes to the compound’s ability to penetrate the blood-brain barrier, enhancing its potential as a therapeutic agent.

Additionally, 2-(3-Phenylpropyl)Pyridine has been investigated for its role in materials science. Its unique electronic properties make it suitable for use in organic semiconductors and light-emitting diodes (OLEDs). Researchers have explored its incorporation into polymer matrices to improve charge transport properties, which is crucial for developing more efficient electronic devices.

The synthesis of 2-(3-Phenylpropyl)Pyridine typically involves multi-step organic reactions, often starting from readily available precursors such as 3-phenylpropanal and pyridine derivatives. Advances in catalytic methods have enabled more efficient and sustainable routes to this compound, reducing the environmental impact of its production. These innovations are essential for scaling up synthesis while maintaining high purity standards.

In conclusion, 2-(3-Phenylpropyl)Pyridine (CAS No. 2110-18-1) is a versatile compound with significant potential across multiple domains of chemistry and pharmacology. Its structural features make it an excellent candidate for further research and development, particularly in the areas of drug discovery and advanced materials. As scientific understanding continues to evolve, the applications of this compound are expected to expand, contributing to advancements in both medicine and technology.

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