Cas no 2172476-12-7 (5-methyl-2,4-bis(propan-2-yl)furan-3-ylmethanamine)

5-Methyl-2,4-bis(propan-2-yl)furan-3-ylmethanamine is a furan-derived amine compound characterized by its substituted furan ring structure. The presence of isopropyl groups at the 2- and 4-positions, along with a methyl group at the 5-position, enhances its steric and electronic properties, making it a potential intermediate in organic synthesis. The amine functional group at the 3-position offers reactivity for further derivatization, enabling applications in pharmaceutical or agrochemical research. Its structural features may contribute to improved stability and selectivity in catalytic or binding interactions. This compound is of interest in specialized synthetic pathways due to its unique scaffold and functional group compatibility.
5-methyl-2,4-bis(propan-2-yl)furan-3-ylmethanamine structure
2172476-12-7 structure
Product Name:5-methyl-2,4-bis(propan-2-yl)furan-3-ylmethanamine
CAS No:2172476-12-7
MF:C12H21NO
MW:195.301243543625
CID:5804276
PubChem ID:165602479
Update Time:2025-11-02

5-methyl-2,4-bis(propan-2-yl)furan-3-ylmethanamine Chemical and Physical Properties

Names and Identifiers

    • 5-methyl-2,4-bis(propan-2-yl)furan-3-ylmethanamine
    • EN300-1615609
    • [5-methyl-2,4-bis(propan-2-yl)furan-3-yl]methanamine
    • 2172476-12-7
    • Inchi: 1S/C12H21NO/c1-7(2)11-9(5)14-12(8(3)4)10(11)6-13/h7-8H,6,13H2,1-5H3
    • InChI Key: LKUVYZIMAXHVDE-UHFFFAOYSA-N
    • SMILES: O1C(C)=C(C(C)C)C(CN)=C1C(C)C

Computed Properties

  • Exact Mass: 195.162314293g/mol
  • Monoisotopic Mass: 195.162314293g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 3
  • Complexity: 179
  • 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: 2.5
  • Topological Polar Surface Area: 39.2?2

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Additional information on 5-methyl-2,4-bis(propan-2-yl)furan-3-ylmethanamine

Comprehensive Guide to 5-methyl-2,4-bis(propan-2-yl)furan-3-ylmethanamine (CAS No. 2172476-12-7): Properties, Applications, and Market Insights

The chemical compound 5-methyl-2,4-bis(propan-2-yl)furan-3-ylmethanamine (CAS No. 2172476-12-7) is an intriguing furan derivative with a unique structural framework. As researchers and industries explore novel organic compounds for diverse applications, this molecule has garnered attention due to its potential in pharmaceuticals, agrochemicals, and material science. This article delves into its chemical properties, synthesis pathways, applications, and emerging trends, while addressing common queries from scientific and industrial communities.

Chemical Structure and Properties: The compound features a furan ring substituted with a methyl group at the 5-position and isopropyl groups at the 2- and 4-positions, with an aminomethyl functional group at the 3-position. This arrangement imparts distinct steric and electronic characteristics, influencing its reactivity and solubility. The presence of the furan core, known for its aromaticity and versatility in organic synthesis, makes this compound a valuable intermediate. Its molecular formula is C12H21NO, with a moderate molecular weight of 195.30 g/mol, suggesting favorable handling and processing properties.

Synthesis and Industrial Relevance: The synthesis of 5-methyl-2,4-bis(propan-2-yl)furan-3-ylmethanamine typically involves multi-step organic reactions, including alkylation and amination of furan precursors. Recent advancements in catalytic methods have improved yields and reduced environmental impact, aligning with the growing demand for sustainable chemistry. Industries are exploring its use in high-performance polymers, where its rigid yet functionalized structure can enhance thermal stability and mechanical properties. Additionally, its potential as a building block for pharmaceutical intermediates is under investigation, particularly in the development of bioactive molecules targeting neurological and metabolic disorders.

Applications in Research and Development: Researchers are leveraging the compound’s unique properties for drug discovery and material innovation. Its furan backbone is amenable to further functionalization, enabling the creation of libraries of derivatives for screening against various biological targets. In material science, its incorporation into polymeric networks has shown promise in improving UV resistance and adhesion properties, making it relevant for coatings and adhesives. The compound’s compatibility with green chemistry principles also positions it as a candidate for eco-friendly industrial applications.

Market Trends and Future Prospects: The global demand for specialized furan derivatives like 5-methyl-2,4-bis(propan-2-yl)furan-3-ylmethanamine is rising, driven by innovations in biodegradable materials and precision medicine. Market analysts highlight its potential in niche sectors such as electronic materials and catalysis, where tailored organic compounds are critical. As regulatory frameworks emphasize safer and sustainable chemicals, this compound’s profile aligns well with industry shifts toward greener alternatives.

Safety and Handling: While not classified as hazardous under standard guidelines, proper laboratory practices should be followed when handling 5-methyl-2,4-bis(propan-2-yl)furan-3-ylmethanamine. Storage in cool, dry conditions and the use of personal protective equipment (PPE) are recommended to ensure safety during research and industrial use.

Conclusion: With its versatile chemistry and broad applicability, 5-methyl-2,4-bis(propan-2-yl)furan-3-ylmethanamine (CAS No. 2172476-12-7) represents a compelling subject for scientific and industrial exploration. Its role in advancing sustainable technologies and bioactive molecule design underscores its relevance in contemporary chemistry. Stay updated with the latest research to uncover new opportunities for this promising compound.

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