Cas no 2057-47-8 (Pyridine,4-[3-phenyl-1-(2-phenylethyl)propyl]-)

Pyridine,4-[3-phenyl-1-(2-phenylethyl)propyl]- structure
2057-47-8 structure
Product Name:Pyridine,4-[3-phenyl-1-(2-phenylethyl)propyl]-
CAS No:2057-47-8
MF:C22H23N
MW:301.42472577095
CID:270739
PubChem ID:74936
Update Time:2025-10-25

Pyridine,4-[3-phenyl-1-(2-phenylethyl)propyl]- Chemical and Physical Properties

Names and Identifiers

    • Pyridine,4-[3-phenyl-1-(2-phenylethyl)propyl]-
    • 4-(1,5-diphenylpentan-3-yl)pyridine
    • 4-(1-PHENETHYL-3-PHENYL-PROPYL)-PYRIDINE
    • EINECS 218-158-6
    • 2057-47-8
    • 4-(1-Phenethyl-3-phenylpropyl)pyridine
    • Pyridine, 4-[3-phenyl-1-(2-phenylethyl)propyl]-
    • Pyridine, 4-(3-phenyl-1-(2-phenylethyl)propyl)-
    • 4-(1-phenethyl-3-phenyl-propyl)pyridine
    • CAA05747
    • AKOS024388287
    • FT-0606975
    • A814708
    • 4-[3-phenyl-1-(2-phenylethyl)propyl]pyridine
    • DTXSID7062160
    • SCHEMBL7145687
    • NS00026690
    • 4-(3-Phenyl-1-(2-phenylethyl)propyl)pyridine
    • Inchi: 1S/C22H23N/c1-3-7-19(8-4-1)11-13-21(22-15-17-23-18-16-22)14-12-20-9-5-2-6-10-20/h1-10,15-18,21H,11-14H2
    • InChI Key: RWNXMNLTEMDVIG-UHFFFAOYSA-N
    • SMILES: N1C=CC(=CC=1)C(CCC1C=CC=CC=1)CCC1C=CC=CC=1

Computed Properties

  • Exact Mass: 301.18300
  • Monoisotopic Mass: 301.183049738g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 23
  • Rotatable Bond Count: 7
  • Complexity: 273
  • 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: 5.9
  • Topological Polar Surface Area: 12.9?2

Experimental Properties

  • PSA: 12.89000
  • LogP: 5.43080

Pyridine,4-[3-phenyl-1-(2-phenylethyl)propyl]- Security Information

  • Hazardous Material transportation number:UN 2810
  • HazardClass:6.1(b)
  • PackingGroup:III
  • Packing Group:III
  • Hazard Level:6.1(b)
  • Safety Term:6.1(b)
  • Packing Group:III

Pyridine,4-[3-phenyl-1-(2-phenylethyl)propyl]- 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%

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Additional information on Pyridine,4-[3-phenyl-1-(2-phenylethyl)propyl]-

Pyridine,4-[3-phenyl-1-(2-phenylethyl)propyl]- (CAS No. 2057-47-8)

Pyridine,4-[3-phenyl-1-(2-phenylethyl)propyl]- (CAS No. 2057-47-8) is a complex organic compound with a unique chemical structure that has garnered significant attention in various fields of research. This compound belongs to the class of pyridines, which are aromatic heterocyclic compounds with a nitrogen atom in the ring. The structure of Pyridine,4-[3-phenyl-1-(2-phenylethyl)propyl]- consists of a pyridine ring substituted at the 4-position with a propyl group that is further substituted with phenyl and 2-phenylethyl groups. This intricate substitution pattern makes it a valuable molecule for exploring chemical reactivity, synthesis techniques, and potential applications in materials science and pharmacology.

Recent studies have highlighted the importance of Pyridine,4-[3-phenyl-1-(2-phenylethyl)propyl]- in the development of advanced materials. Researchers have investigated its ability to act as a precursor for the synthesis of novel polymers and coordination compounds. For instance, its nitrogen-containing aromatic ring can participate in π-interactions and hydrogen bonding, making it suitable for applications in molecular recognition and sensing technologies. Furthermore, its bulky substituents provide steric hindrance, which can be exploited to design materials with tailored mechanical and electronic properties.

In the field of pharmacology, Pyridine,4-[3-phenyl-1-(2-phenylethyl)propyl]- has been studied as a potential lead compound for drug discovery. Its structure resembles certain bioactive molecules, suggesting that it could serve as a scaffold for developing new therapeutic agents. Recent research has focused on its ability to inhibit specific enzymes and modulate cellular pathways, which could have implications in treating diseases such as cancer and neurodegenerative disorders.

The synthesis of Pyridine,4-[3-phenyl-1-(2-phenylethyl)propyl]- involves multi-step organic reactions that require precise control over reaction conditions. One common approach is the use of Suzuki-Miyaura coupling reactions to assemble the aromatic substituents onto the pyridine ring. This method allows for high regioselectivity and enables the construction of complex molecular architectures. Additionally, researchers have explored alternative synthetic routes using transition metal catalysts to improve yield and efficiency.

From an environmental perspective, Pyridine,4-[3-phenyl-1-(2-phenylethyl)propyl]- has been studied for its biodegradability and potential impact on ecosystems. Initial findings suggest that it undergoes slow degradation under aerobic conditions due to its stable aromatic structure. However, further research is needed to fully understand its environmental fate and develop strategies for mitigating any adverse effects.

In conclusion, Pyridine,4-[3-phenyl-1-(2-ph enethyl)prop yl]- (CAS No. 2057 - 47 - 8 ) is a versatile compound with promising applications across multiple disciplines. Its unique chemical structure provides opportunities for innovation in materials science , pharmacology , and environmental chemistry . As research continues to uncover new properties and uses , this compound is expected to play an increasingly important role in advancing scientific knowledge and technological applications .

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