Cas no 80493-89-6 (BENZONITRILE, 4-(6-METHOXY-2-NAPHTHALENYL)-)

4-(6-Methoxy-2-naphthalenyl)benzonitrile is a specialized organic compound featuring a benzonitrile core substituted with a 6-methoxy-2-naphthalenyl group. This structure imparts unique electronic and steric properties, making it valuable in synthetic chemistry and materials science applications. The methoxy and naphthalene groups enhance its utility as an intermediate in the synthesis of advanced organic materials, including liquid crystals, pharmaceuticals, and optoelectronic compounds. Its rigid aromatic framework contributes to thermal stability and controlled reactivity, facilitating precise modifications in target molecules. The compound is typically handled under standard laboratory conditions, requiring protection from light and moisture to maintain purity. Its well-defined structure ensures reproducibility in research and industrial processes.
BENZONITRILE, 4-(6-METHOXY-2-NAPHTHALENYL)- structure
80493-89-6 structure
Product Name:BENZONITRILE, 4-(6-METHOXY-2-NAPHTHALENYL)-
CAS No:80493-89-6
MF:C18H13NO
MW:259.301924467087
CID:3394163
PubChem ID:13450017
Update Time:2025-05-22

BENZONITRILE, 4-(6-METHOXY-2-NAPHTHALENYL)- Chemical and Physical Properties

Names and Identifiers

    • BENZONITRILE, 4-(6-METHOXY-2-NAPHTHALENYL)-
    • 4-(6-METHOXY-NAPHTHALEN-2-YL)-BENZONITRILE
    • VCA44550
    • 80493-89-6
    • 4-(6-Methoxynaphthalen-2-yl)benzonitrile
    • MDL: MFCD08457012
    • Inchi: 1S/C18H13NO/c1-20-18-9-8-16-10-15(6-7-17(16)11-18)14-4-2-13(12-19)3-5-14/h2-11H,1H3
    • InChI Key: DLCUCSUSEOKTCX-UHFFFAOYSA-N
    • SMILES: O(C)C1C=CC2=CC(=CC=C2C=1)C1C=CC(C#N)=CC=1

Computed Properties

  • Exact Mass: 259.099714038g/mol
  • Monoisotopic Mass: 259.099714038g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 20
  • Rotatable Bond Count: 2
  • Complexity: 363
  • 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: 4.5
  • Topological Polar Surface Area: 33?2

BENZONITRILE, 4-(6-METHOXY-2-NAPHTHALENYL)- Pricemore >>

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BENZONITRILE, 4-(6-METHOXY-2-NAPHTHALENYL)- Related Literature

Additional information on BENZONITRILE, 4-(6-METHOXY-2-NAPHTHALENYL)-

BENZONITRILE, 4-(6-METHOXY-2-NAPHTHALENYL)- (CAS No. 80493-89-6): A Comprehensive Overview

BENZONITRILE, 4-(6-METHOXY-2-NAPHTHALENYL)-, with the CAS No. 80493-89-6, is a specialized organic compound that has garnered significant attention in the fields of pharmaceuticals, materials science, and chemical research. This compound, characterized by its unique naphthalene and benzonitrile structure, serves as a crucial intermediate in the synthesis of various high-value chemicals. Its molecular formula is C18H13NO, and it is known for its versatile applications, particularly in the development of advanced materials and bioactive molecules.

The compound's structure features a 6-methoxy-2-naphthalenyl group attached to a benzonitrile moiety, which imparts distinct chemical properties. This combination enhances its utility in organic synthesis, where it acts as a building block for more complex molecules. Researchers and industries value BENZONITRILE, 4-(6-METHOXY-2-NAPHTHALENYL)- for its stability, reactivity, and ability to participate in various coupling reactions, making it a sought-after compound in modern chemistry.

One of the most prominent applications of CAS No. 80493-89-6 is in the pharmaceutical industry. The compound's naphthalene core is a common motif in drug design, particularly in the development of anti-inflammatory and anticancer agents. Recent studies have explored its potential as a precursor for novel therapeutics, aligning with the growing demand for innovative treatments in healthcare. This has led to increased interest in the compound's synthesis and optimization, as researchers seek to unlock its full potential.

In addition to pharmaceuticals, BENZONITRILE, 4-(6-METHOXY-2-NAPHTHALENYL)- finds applications in materials science. Its aromatic structure and electron-rich properties make it suitable for use in organic semiconductors and light-emitting diodes (OLEDs). With the rise of sustainable technologies, the demand for high-performance organic materials has surged, positioning this compound as a valuable component in next-generation electronic devices.

The synthesis of BENZONITRILE, 4-(6-METHOXY-2-NAPHTHALENYL)- typically involves multi-step organic reactions, including palladium-catalyzed cross-coupling and nitrile formation. These methods have been refined over the years to improve yield and purity, addressing the needs of industrial and academic researchers. Recent advancements in green chemistry have also influenced the synthesis protocols, with a focus on reducing hazardous byproducts and improving efficiency.

Market trends indicate a steady growth in the demand for CAS No. 80493-89-6, driven by its expanding applications. The compound is commercially available through specialized chemical suppliers, catering to the needs of research institutions and manufacturing units. Pricing and availability may vary based on purity and scale, but its niche market ensures consistent interest from buyers worldwide.

From an environmental and safety perspective, BENZONITRILE, 4-(6-METHOXY-2-NAPHTHALENYL)- is handled with standard laboratory precautions. While it is not classified as highly hazardous, proper storage and handling are essential to maintain its integrity and ensure user safety. Regulatory compliance varies by region, but the compound generally falls under standard chemical safety guidelines.

Looking ahead, the future of BENZONITRILE, 4-(6-METHOXY-2-NAPHTHALENYL)- appears promising. Ongoing research into its derivatives and applications is likely to uncover new opportunities, particularly in drug discovery and advanced materials. As industries continue to prioritize innovation and sustainability, this compound is poised to play a pivotal role in shaping the next wave of chemical advancements.

In summary, CAS No. 80493-89-6 represents a versatile and valuable compound with broad applications across multiple sectors. Its unique chemical properties, coupled with its role in cutting-edge research, make it a subject of enduring interest. Whether in pharmaceuticals, materials science, or organic synthesis, BENZONITRILE, 4-(6-METHOXY-2-NAPHTHALENYL)- continues to demonstrate its significance in the ever-evolving landscape of chemistry.

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