Cas no 1529-40-4 (9H-Fluorene-9-carbonitrile)

9H-Fluorene-9-carbonitrile is a versatile organic compound characterized by its fluorene backbone and nitrile functional group. This structure imparts unique electronic and steric properties, making it valuable in organic synthesis, particularly as a precursor for pharmaceuticals, agrochemicals, and advanced materials. Its rigid, planar fluorene core enhances stability and conjugation, while the nitrile group offers reactivity for further functionalization. The compound is often employed in cross-coupling reactions, polymerization initiators, and as a building block for optoelectronic materials. High purity grades ensure consistent performance in research and industrial applications. Its balanced reactivity and structural features make it a practical choice for synthetic chemists seeking tailored molecular architectures.
9H-Fluorene-9-carbonitrile structure
9H-Fluorene-9-carbonitrile structure
Product Name:9H-Fluorene-9-carbonitrile
CAS No:1529-40-4
MF:C14H9N
MW:191.227963209152
CID:173763
PubChem ID:73721
Update Time:2025-11-01

9H-Fluorene-9-carbonitrile Chemical and Physical Properties

Names and Identifiers

    • 9H-Fluorene-9-carbonitrile
    • 9-Cyan-fluoren
    • 9-Cyanofluorene
    • 9-Fluorencarbonitril
    • 9-Fluorenonitrile
    • 9-Fluorenylnitril
    • Fluoren-9-carbonitril
    • Fluorene-9-carbonitrile
    • FT-0767812
    • 1529-40-4
    • NSC-126783
    • NS00044402
    • NSC 126783
    • EINECS 216-212-3
    • CS-0237021
    • NSC126783
    • AKOS006273102
    • 9-cyano-fluorene
    • DTXSID50165153
    • 1-Ethyl-1-tosylmethylisocyanide
    • Z1198154238
    • SCHEMBL6648437
    • EN300-176706
    • BAA52940
    • AS-82607
    • Inchi: 1S/C14H9N/c15-9-14-12-7-3-1-5-10(12)11-6-2-4-8-13(11)14/h1-8,14H
    • InChI Key: CJVMCKCMPQEKPZ-UHFFFAOYSA-N
    • SMILES: N#CC1C2C=CC=CC=2C2C=CC=CC1=2

Computed Properties

  • Exact Mass: 191.07300
  • Monoisotopic Mass: 191.073499291g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 0
  • Complexity: 265
  • 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: 3
  • Topological Polar Surface Area: 23.8?2

Experimental Properties

  • PSA: 23.79000
  • LogP: 3.32248

9H-Fluorene-9-carbonitrile Customs Data

  • HS CODE:2926909090
  • Customs Data:

    China Customs Code:

    2926909090

    Overview:

    2926909090 Other nitrile based compounds. VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:6.5% general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    HS:2926909090 other nitrile-function compounds VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

9H-Fluorene-9-carbonitrile Pricemore >>

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$ 50.00 2022-06-05
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9H-Fluorene-9-carbonitrile Related Literature

Additional information on 9H-Fluorene-9-carbonitrile

Recent Advances in the Study of 9H-Fluorene-9-carbonitrile (CAS: 1529-40-4) and Its Applications in Chemical Biology and Medicine

9H-Fluorene-9-carbonitrile (CAS: 1529-40-4) is a versatile organic compound with a fluorene backbone and a nitrile functional group. This compound has garnered significant attention in recent years due to its potential applications in chemical biology, medicinal chemistry, and materials science. The unique structural features of 9H-Fluorene-9-carbonitrile make it a promising scaffold for the development of novel pharmaceuticals, fluorescent probes, and organic electronic materials. This research brief aims to summarize the latest findings and advancements related to this compound, focusing on its synthesis, biological activities, and potential therapeutic applications.

Recent studies have explored the synthetic routes to 9H-Fluorene-9-carbonitrile, with an emphasis on green chemistry approaches. A 2023 publication in the Journal of Organic Chemistry reported a novel, one-pot synthesis method using palladium-catalyzed C-H activation, which significantly improved the yield and reduced the environmental impact compared to traditional methods. This advancement is particularly relevant for large-scale production, as it addresses the growing demand for sustainable chemical processes in the pharmaceutical industry.

In the realm of medicinal chemistry, 9H-Fluorene-9-carbonitrile has been investigated as a core structure for designing kinase inhibitors. A recent study published in Bioorganic & Medicinal Chemistry Letters demonstrated that derivatives of this compound exhibit potent inhibitory activity against cyclin-dependent kinases (CDKs), which are key targets in cancer therapy. The researchers identified specific structural modifications that enhance binding affinity and selectivity, paving the way for the development of next-generation anticancer agents.

Another exciting application of 9H-Fluorene-9-carbonitrile lies in its use as a fluorescent probe for bioimaging. A 2024 study in ACS Chemical Biology highlighted its utility in detecting reactive oxygen species (ROS) in live cells. The compound's inherent fluorescence properties, combined with its ability to selectively react with ROS, make it a valuable tool for studying oxidative stress-related diseases, such as neurodegenerative disorders and cardiovascular conditions.

Beyond its biological applications, 9H-Fluorene-9-carbonitrile has also shown promise in materials science. Research published in Advanced Materials in early 2024 revealed its potential as a building block for organic semiconductors. The compound's rigid, planar structure and electron-withdrawing nitrile group contribute to excellent charge transport properties, making it suitable for use in organic light-emitting diodes (OLEDs) and photovoltaic devices.

In conclusion, 9H-Fluorene-9-carbonitrile (CAS: 1529-40-4) represents a multifaceted compound with diverse applications across chemical biology and medicine. Recent advancements in its synthesis, biological evaluation, and material applications underscore its growing importance in scientific research. Future studies should focus on further optimizing its properties and exploring new therapeutic and technological applications to fully realize its potential.

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