Cas no 403615-62-3 (Cyclobutanecarbonitrile,1-acetyl-)

Cyclobutanecarbonitrile,1-acetyl- is a specialized organic compound featuring a cyclobutane ring substituted with both a nitrile and an acetyl functional group. This structure imparts unique reactivity, making it valuable in synthetic organic chemistry, particularly in the construction of complex heterocycles and pharmaceutical intermediates. The presence of the nitrile group offers versatility for further functionalization through hydrolysis, reduction, or nucleophilic addition, while the acetyl moiety provides a handle for condensation or substitution reactions. Its rigid cyclobutane backbone may also contribute to steric constraints, useful in stereoselective synthesis. The compound is typically employed in research and fine chemical applications where precise molecular architecture is required.
Cyclobutanecarbonitrile,1-acetyl- structure
403615-62-3 structure
Product Name:Cyclobutanecarbonitrile,1-acetyl-
CAS No:403615-62-3
MF:C7H9NO
MW:123.152461767197
CID:325924
PubChem ID:45085166
Update Time:2025-06-15

Cyclobutanecarbonitrile,1-acetyl- Chemical and Physical Properties

Names and Identifiers

    • Cyclobutanecarbonitrile,1-acetyl-
    • Cyclobutanecarbonitrile, 1-acetyl- (9CI)
    • 403615-62-3
    • Cyclobutanecarbonitrile,1-acetyl-(9ci)
    • SCHEMBL16478723
    • 1-Acetylcyclobutanecarbonitrile
    • cyclobutanecarbonitrile, 1-acetyl-
    • 1-ACETYLCYCLOBUTANE-1-CARBONITRILE
    • EN300-7288856
    • Inchi: 1S/C7H9NO/c1-6(9)7(5-8)3-2-4-7/h2-4H2,1H3
    • InChI Key: SAFDHKQOQGFNTL-UHFFFAOYSA-N
    • SMILES: O=C(C)C1(C#N)CCC1

Computed Properties

  • Exact Mass: 123.068413911g/mol
  • Monoisotopic Mass: 123.068413911g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 1
  • Complexity: 182
  • 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: 0.7
  • Topological Polar Surface Area: 40.9?2

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Cyclobutanecarbonitrile,1-acetyl- Related Literature

Additional information on Cyclobutanecarbonitrile,1-acetyl-

Comprehensive Overview of Cyclobutanecarbonitrile,1-acetyl- (CAS No. 403615-62-3)

Cyclobutanecarbonitrile,1-acetyl- (CAS No. 403615-62-3) is a specialized organic compound that has garnered significant attention in the fields of pharmaceutical research, agrochemical development, and material science. This nitrile derivative, characterized by its cyclobutane ring and acetyl functional group, exhibits unique chemical properties that make it a valuable intermediate in synthetic chemistry. Researchers and industry professionals frequently search for terms like "Cyclobutanecarbonitrile synthesis", "1-acetyl-cyclobutanecarbonitrile applications", and "CAS 403615-62-3 properties", reflecting its growing relevance in advanced chemical applications.

The molecular structure of Cyclobutanecarbonitrile,1-acetyl- combines the stability of a cyclobutane framework with the reactivity of a nitrile group, enabling diverse transformations. Recent studies highlight its role in developing novel heterocyclic compounds, a trending topic in drug discovery. Searches for "nitrile-based drug intermediates" and "cyclobutane derivatives in medicine" underscore the compound's potential in addressing challenges like antibiotic resistance and targeted cancer therapies. Its compatibility with green chemistry principles—another hot topic—further enhances its appeal for sustainable manufacturing.

From a technical perspective, Cyclobutanecarbonitrile,1-acetyl- demonstrates notable solubility in polar organic solvents, a feature often queried as "solubility of CAS 403615-62-3". This property facilitates its use in catalytic reactions and polymer modifications, areas where precision and efficiency are critical. Analytical techniques such as NMR spectroscopy and mass spectrometry are commonly employed to verify its purity, addressing frequent search queries like "characterization of 1-acetyl-cyclobutanecarbonitrile".

Innovations in material science have also leveraged this compound, particularly in designing high-performance polymers with enhanced thermal stability. Industry forums often discuss "cyclobutane nitriles in advanced materials", aligning with the surge in demand for lightweight, durable composites. Furthermore, its role in flavor and fragrance chemistry—answering niche searches such as "nitrile compounds in perfumery"—demonstrates its cross-industry versatility.

Quality control protocols for Cyclobutanecarbonitrile,1-acetyl- emphasize strict adherence to international standards like ISO and REACH, addressing concerns about "regulatory compliance for CAS 403615-62-3". Suppliers frequently highlight batch-to-batch consistency, a key consideration for buyers searching "reliable 1-acetyl-cyclobutanecarbonitrile suppliers". Storage recommendations typically focus on inert atmospheres and moisture-free conditions, topics often explored under "handling cyclobutane derivatives safely".

Emerging applications in electronic chemicals and photoactive materials have further expanded the compound's market potential. Recent patents referencing 403615-62-3 reveal its utility in organic semiconductors, a response to the booming interest in "flexible electronics" and "renewable energy technologies". Such developments align with global trends toward sustainable innovation, making this compound a subject of ongoing research and commercial interest.

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