Cas no 103906-20-3 (2-(1-Ethylpropyl)piperidine)

2-(1-Ethylpropyl)piperidine is a substituted piperidine derivative characterized by its branched alkyl side chain at the 2-position. This structural feature enhances its lipophilicity, making it a valuable intermediate in organic synthesis and pharmaceutical research. The compound's steric and electronic properties can influence reactivity in catalytic processes or serve as a building block for bioactive molecules. Its well-defined molecular structure allows for precise modifications, facilitating applications in medicinal chemistry, particularly in the development of amine-based therapeutics. The compound is typically handled under inert conditions due to its sensitivity to oxidation. High purity grades are available for research and industrial use.
2-(1-Ethylpropyl)piperidine structure
2-(1-Ethylpropyl)piperidine structure
Product Name:2-(1-Ethylpropyl)piperidine
CAS No:103906-20-3
MF:C10H21N
MW:155.28044295311
MDL:MFCD02663646
CID:3056163
PubChem ID:4527381
Update Time:2025-11-02

2-(1-Ethylpropyl)piperidine Chemical and Physical Properties

Names and Identifiers

    • 2-(1-Ethylpropyl)piperidine
    • 2-(pentan-3-yl)piperidine
    • 103906-20-3
    • BBL020930
    • EN300-1233863
    • 2-(1-Ethylpropyl)piperidine, AldrichCPR
    • BS-29971
    • SCHEMBL21567213
    • STK893636
    • 2-pentan-3-ylpiperidine
    • AKOS001476537
    • MFCD02663646
    • MDL: MFCD02663646
    • Inchi: 1S/C10H21N/c1-3-9(4-2)10-7-5-6-8-11-10/h9-11H,3-8H2,1-2H3
    • InChI Key: WDIGSSBTCZVWBL-UHFFFAOYSA-N
    • SMILES: N1CCCCC1C(CC)CC

Computed Properties

  • Exact Mass: 155.167399674Da
  • Monoisotopic Mass: 155.167399674Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 3
  • Complexity: 97
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.8
  • Topological Polar Surface Area: 12?2

2-(1-Ethylpropyl)piperidine Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
E938475-50mg
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$ 50.00 2022-06-05
TRC
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$ 95.00 2022-06-05
TRC
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$ 320.00 2022-06-05
Apollo Scientific
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£115.00 2025-02-21
Apollo Scientific
OR905802-1g
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A2B Chem LLC
AI06197-100mg
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$271.00 2024-04-20
A2B Chem LLC
AI06197-250mg
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$532.00 2024-04-20
abcr
AB382951-250 mg
2-(Pentan-3-yl)piperidine
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€144.00 2022-03-02
abcr
AB382951-250mg
2-(Pentan-3-yl)piperidine; .
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Enamine
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2-(1-Ethylpropyl)piperidine Related Literature

Additional information on 2-(1-Ethylpropyl)piperidine

2-(1-Ethylpropyl)piperidine (CAS No. 103906-20-3): A Comprehensive Overview of Properties and Applications

2-(1-Ethylpropyl)piperidine (CAS No. 103906-20-3) is a specialized organic compound that has garnered significant attention in various scientific and industrial applications. This piperidine derivative, characterized by its unique ethylpropyl substitution pattern, offers distinct chemical properties that make it valuable in multiple fields. With the growing interest in heterocyclic compounds and their applications, 2-(1-Ethylpropyl)piperidine stands out as a compound of interest for researchers and industry professionals alike.

The molecular structure of 2-(1-Ethylpropyl)piperidine features a piperidine ring substituted at the 2-position with a 1-ethylpropyl group. This configuration imparts specific steric and electronic characteristics to the molecule, influencing its reactivity and interactions. The compound's CAS number 103906-20-3 serves as a unique identifier in chemical databases, ensuring accurate referencing in research and commercial contexts. As the demand for specialty chemicals continues to rise, understanding the properties of compounds like 2-(1-Ethylpropyl)piperidine becomes increasingly important.

Recent trends in chemical research highlight the importance of nitrogen-containing heterocycles, with piperidine derivatives being particularly prominent. 2-(1-Ethylpropyl)piperidine fits into this category, offering potential applications in areas such as pharmaceutical intermediates, catalysis, and material science. The compound's balanced lipophilicity, influenced by its ethylpropyl side chain, makes it an interesting candidate for various formulation applications. Researchers are particularly interested in how modifications to the piperidine scaffold can lead to compounds with tailored properties for specific uses.

In the pharmaceutical sector, 2-(1-Ethylpropyl)piperidine serves as a valuable building block for more complex molecules. The piperidine moiety is a common structural element in many bioactive compounds, and the addition of the 1-ethylpropyl group can significantly alter the pharmacokinetic properties of resulting molecules. While not a drug substance itself, this compound's role in medicinal chemistry research continues to grow, particularly in the development of central nervous system-targeting agents and other specialized therapeutics.

The synthesis of 2-(1-Ethylpropyl)piperidine typically involves organic synthesis techniques that allow for the selective introduction of the ethylpropyl substituent. Modern synthetic approaches emphasize atom economy and green chemistry principles, reflecting the broader industry shift toward sustainable practices. Researchers are exploring various catalytic systems to optimize the production of this and related piperidine derivatives, with particular attention to yield, purity, and environmental impact.

From a commercial perspective, 2-(1-Ethylpropyl)piperidine (CAS 103906-20-3) occupies a niche but important position in the fine chemicals market. Suppliers typically offer this compound in various purity grades, from technical to high-purity research grades, catering to different application needs. The global market for such specialty piperidine compounds shows steady growth, driven by increasing research activities and industrial applications across multiple sectors.

Quality control for 2-(1-Ethylpropyl)piperidine involves standard analytical techniques including gas chromatography, mass spectrometry, and NMR spectroscopy. These methods ensure the compound meets the required specifications for various applications. Proper handling and storage conditions are essential to maintain the integrity of this chemical, with recommendations typically including protection from moisture and storage under inert atmosphere when necessary.

Looking to the future, research into 2-(1-Ethylpropyl)piperidine and related compounds continues to evolve. Emerging applications in advanced materials and catalysis are particularly promising areas of investigation. The compound's structural features make it a candidate for incorporation into novel polymeric materials or as a ligand in catalytic systems. As synthetic methodologies advance and analytical techniques become more sophisticated, our understanding of this compound's full potential will undoubtedly expand.

For researchers and industry professionals seeking information about 2-(1-Ethylpropyl)piperidine (CAS 103906-20-3), it's important to consult reliable sources and suppliers. The compound's technical data sheets provide essential information about its physical properties, handling requirements, and potential applications. As with any specialized chemical, proper safety assessments should be conducted prior to use, following all relevant guidelines and regulations.

The scientific literature contains numerous references to piperidine derivatives and their applications, with 2-(1-Ethylpropyl)piperidine representing an interesting case study in how subtle structural modifications can lead to significant changes in properties and applications. Ongoing research continues to uncover new potential uses for this versatile compound, ensuring its place in the toolkit of modern chemistry.

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