Cas no 27287-82-7 (Propanedinitrile,2-(1-pyrenylmethylene)-)

Propanedinitrile,2-(1-pyrenylmethylene)- is a fluorescent organic compound characterized by its pyrene-based structure, which imparts strong photophysical properties. This compound is notable for its high quantum yield and stability, making it suitable for applications in optoelectronics, molecular probes, and fluorescence labeling. Its extended π-conjugation system enhances absorption and emission characteristics, enabling sensitive detection in analytical and imaging techniques. The compound’s rigid molecular framework contributes to its thermal and chemical robustness, ensuring reliability in diverse experimental conditions. Researchers value its tunable electronic properties, which facilitate customization for specific photochemical or material science applications.
Propanedinitrile,2-(1-pyrenylmethylene)- structure
27287-82-7 structure
Product Name:Propanedinitrile,2-(1-pyrenylmethylene)-
CAS No:27287-82-7
MF:C20H10N2
MW:278.306804180145
CID:282391
PubChem ID:290168
Update Time:2025-05-21

Propanedinitrile,2-(1-pyrenylmethylene)- Chemical and Physical Properties

Names and Identifiers

    • Propanedinitrile,2-(1-pyrenylmethylene)-
    • 2-(pyren-1-ylmethylidene)propanedinitrile
    • (pyren-1-ylmethylene)malononitrile
    • (pyren-1-ylmethylidene)propanedinitrile
    • 1-dicyanovinylpyrene
    • AC1L6DBK
    • AC1Q4PYV
    • AR-1A7796
    • CTK4F9405
    • KST-1A3379
    • NSC153129
    • 2-[(pyren-1-yl)methylidene]propanedinitrile
    • 27287-82-7
    • 2-(Pyren-1-ylmethylene)malononitrile
    • KQRUQVGUIFJRBU-UHFFFAOYSA-N
    • 2-(1-Pyrenylmethylene)-malononitrile
    • J-505408
    • SCHEMBL11649829
    • NSC-153129
    • starbld0009161
    • DTXSID30302726
    • Inchi: 1S/C20H10N2/c21-11-13(12-22)10-17-7-6-16-5-4-14-2-1-3-15-8-9-18(17)20(16)19(14)15/h1-10H
    • InChI Key: KQRUQVGUIFJRBU-UHFFFAOYSA-N
    • SMILES: N#C/C(/C#N)=C/C1C=CC2=CC=C3C=CC=C4C=CC=1C2=C43

Computed Properties

  • Exact Mass: 278.0845
  • Monoisotopic Mass: 278.084398327g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 22
  • Rotatable Bond Count: 1
  • Complexity: 553
  • 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: 5.1
  • Topological Polar Surface Area: 47.6?2

Experimental Properties

  • PSA: 47.58
  • LogP: 5.01456

Propanedinitrile,2-(1-pyrenylmethylene)- Pricemore >>

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Additional information on Propanedinitrile,2-(1-pyrenylmethylene)-

Comprehensive Overview of Propanedinitrile,2-(1-pyrenylmethylene)- (CAS No. 27287-82-7)

Propanedinitrile,2-(1-pyrenylmethylene)- (CAS No. 27287-82-7) is a specialized organic compound that has garnered significant attention in the fields of materials science and photochemistry. This compound, characterized by its unique pyrene-based structure, is widely studied for its fluorescent properties and potential applications in optoelectronic devices. Researchers and industry professionals are increasingly interested in its synthesis, properties, and practical uses, making it a hot topic in contemporary scientific discussions.

The molecular structure of Propanedinitrile,2-(1-pyrenylmethylene)- combines a pyrene moiety with a dinitrile group, resulting in a compound that exhibits strong absorption and emission spectra. These characteristics make it particularly valuable for applications such as organic light-emitting diodes (OLEDs) and solar cells. With the growing demand for sustainable energy solutions, this compound's role in renewable energy technologies is a key area of exploration.

One of the most frequently searched questions about Propanedinitrile,2-(1-pyrenylmethylene)- revolves around its synthesis methods. The compound is typically prepared through a Knoevenagel condensation reaction, which involves the reaction of pyrene-1-carbaldehyde with malononitrile. This process is well-documented in the literature, but recent advancements have focused on optimizing yield and purity to meet industrial standards. Researchers are also investigating green chemistry approaches to reduce environmental impact during synthesis.

In addition to its optoelectronic applications, Propanedinitrile,2-(1-pyrenylmethylene)- is being explored for its potential in biological imaging. Its fluorescence stability and compatibility with biological systems make it a promising candidate for bioimaging probes. This aligns with the broader trend of integrating advanced materials into medical diagnostics and therapeutics, a topic that resonates strongly with both academic and commercial audiences.

The compound's thermal stability and solubility are also critical factors for its practical use. Recent studies have highlighted its performance in various solvents, which is essential for formulating inks or coatings in printed electronics. As the demand for flexible and wearable electronics grows, the relevance of Propanedinitrile,2-(1-pyrenylmethylene)- in this sector is expected to rise significantly.

Another area of interest is the compound's potential in sensor technologies. Its ability to interact with specific analytes and produce measurable fluorescence changes makes it suitable for detecting environmental pollutants or biochemical markers. This application is particularly relevant in the context of increasing global concerns about environmental monitoring and health safety.

From a commercial perspective, the availability and pricing of Propanedinitrile,2-(1-pyrenylmethylene)- are frequently discussed topics. Suppliers often provide this compound in high purity grades for research and development purposes. However, scaling up production to meet industrial demands remains a challenge, prompting ongoing research into cost-effective synthesis routes.

In summary, Propanedinitrile,2-(1-pyrenylmethylene)- (CAS No. 27287-82-7) is a versatile compound with wide-ranging applications in optoelectronics, bioimaging, and sensor technologies. Its unique properties and alignment with current technological trends ensure its continued relevance in scientific and industrial communities. As research progresses, new applications and improved synthesis methods are likely to emerge, further solidifying its importance in advanced materials science.

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