Cas no 248-96-4 (5H-Naphtho[2,3-b]carbazole)

5H-Naphtho[2,3-b]carbazole structure
5H-Naphtho[2,3-b]carbazole structure
Product Name:5H-Naphtho[2,3-b]carbazole
CAS No:248-96-4
MF:C20H13N
MW:267.323924779892
CID:264818
PubChem ID:136057
Update Time:2025-04-24

5H-Naphtho[2,3-b]carbazole Chemical and Physical Properties

Names and Identifiers

    • 5H-Naphtho[2,3-b]carbazole
    • Naphtho[2,3-b]carbazole
    • SCHEMBL15103897
    • MEXWZXCQQQYPNG-UHFFFAOYSA-N
    • Naphtho(2,3-b)carbazole
    • 248-96-4
    • DTXSID50179497
    • Inchi: 1S/C20H13N/c1-2-6-14-10-16-12-20-18(11-15(16)9-13(14)5-1)17-7-3-4-8-19(17)21-20/h1-12,21H
    • InChI Key: MEXWZXCQQQYPNG-UHFFFAOYSA-N
    • SMILES: N1C2C=CC=CC=2C2C=C3C=C4C=CC=CC4=CC3=CC1=2

Computed Properties

  • Exact Mass: 266.09706
  • Monoisotopic Mass: 267.104799419g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 0
  • Heavy Atom Count: 21
  • Rotatable Bond Count: 0
  • Complexity: 391
  • 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: 5.3
  • Topological Polar Surface Area: 15.8?2

Experimental Properties

  • PSA: 12.89

5H-Naphtho[2,3-b]carbazole Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Alichem
A449038169-1g
5H-Naphtho[2,3-b]carbazole
248-96-4 95%
1g
$1431.17 2023-09-02
Alichem
A449038169-5g
5H-Naphtho[2,3-b]carbazole
248-96-4 95%
5g
$3827.04 2023-09-02

Additional information on 5H-Naphtho[2,3-b]carbazole

5H-Naphtho[2,3-b]carbazole (CAS 248-96-4): A Versatile Polycyclic Aromatic Compound with Emerging Applications

5H-Naphtho[2,3-b]carbazole (CAS 248-96-4) is a fascinating polycyclic aromatic compound that has garnered significant attention in recent years due to its unique structural properties and potential applications in advanced materials. As researchers explore novel organic semiconductors and luminescent materials, this naphthocarbazole derivative stands out for its remarkable electronic characteristics and thermal stability.

The molecular structure of 5H-Naphtho[2,3-b]carbazole features a fused system of three aromatic rings, creating an extended π-conjugated system that enables interesting photophysical properties. This structural feature makes it particularly valuable in the development of organic light-emitting diodes (OLEDs) and other optoelectronic devices, which are currently hot topics in materials science research.

Recent studies have highlighted the potential of naphthocarbazole-based materials in energy-related applications. The compound's ability to form stable thin films and its favorable charge transport properties make it a promising candidate for organic photovoltaic cells, addressing the growing demand for renewable energy solutions. Researchers are particularly interested in how modifications to the 5H-Naphtho[2,3-b]carbazole structure can tune its electronic properties for specific applications.

In the pharmaceutical field, while not directly used as an active ingredient, the naphthocarbazole scaffold serves as an important structural motif in drug discovery. Medicinal chemists value its rigid, planar structure for designing molecules that can interact with biological targets. This has led to increased interest in CAS 248-96-4 as a building block for more complex therapeutic agents.

The synthesis and purification of 5H-Naphtho[2,3-b]carbazole require specialized expertise in organic chemistry. Modern synthetic approaches focus on improving yields and reducing environmental impact, aligning with the principles of green chemistry that are currently emphasized across the chemical industry. Advanced purification techniques ensure the high purity required for electronic applications.

From an analytical perspective, characterizing naphthocarbazole derivatives involves sophisticated techniques such as high-performance liquid chromatography (HPLC), nuclear magnetic resonance (NMR) spectroscopy, and mass spectrometry. These methods are crucial for quality control, especially when the compound is used in sensitive applications like organic electronics.

The thermal stability of 5H-Naphtho[2,3-b]carbazole makes it particularly valuable for high-temperature applications. Recent studies have investigated its behavior under various thermal conditions, providing important data for engineers designing devices that must operate in demanding environments. This property is especially relevant for the next-generation display technologies currently under development.

In materials science, researchers are exploring the use of CAS 248-96-4 in the creation of novel polymers and small-molecule semiconductors. The compound's ability to facilitate charge transport while maintaining stability makes it attractive for flexible electronics, a rapidly growing sector responding to demands for wearable technology and foldable devices.

Environmental considerations are increasingly important in chemical research, and studies on naphthocarbazole compounds include assessments of their ecological impact. While 5H-Naphtho[2,3-b]carbazole itself shows good stability, researchers are developing more sustainable production methods and investigating its biodegradation pathways.

The commercial availability of 5H-Naphtho[2,3-b]carbazole has improved in recent years as demand grows from academic and industrial researchers. Suppliers now offer various purity grades tailored to different applications, from basic research to high-performance electronic materials. This accessibility supports innovation across multiple disciplines.

Looking to the future, naphthocarbazole chemistry continues to evolve with new derivatives being synthesized and characterized. The unique properties of 5H-Naphtho[2,3-b]carbazole ensure it will remain an important compound in the development of advanced materials, particularly as society moves toward more sustainable and efficient technologies.

For researchers interested in working with CAS 248-96-4, it's important to consult the latest literature on handling and applications. While the compound itself is not classified as hazardous, proper laboratory practices should always be followed when working with polycyclic aromatic compounds to ensure safety and obtain reliable results.

The scientific community continues to uncover new potential applications for 5H-Naphtho[2,3-b]carbazole, from advanced coatings to specialized sensors. Its versatility and the growing understanding of its properties suggest that this compound will play an increasingly important role in materials science and related fields in the coming years.

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