Cas no 2417-77-8 (9-(Bromomethyl)anthracene)

9-(Bromomethyl)anthracene is a brominated derivative of anthracene, commonly utilized as a versatile intermediate in organic synthesis. Its key advantages include its high reactivity as an alkylating agent, enabling efficient functionalization of anthracene frameworks for applications in materials science and pharmaceuticals. The bromomethyl group facilitates further derivatization, making it valuable for cross-coupling reactions, polymer synthesis, and the preparation of fluorescent dyes or optoelectronic materials. The compound exhibits good stability under standard conditions, ensuring reliable handling and storage. Its well-defined structure and consistent purity make it a preferred choice for researchers requiring precise modifications of anthracene-based systems.
9-(Bromomethyl)anthracene structure
9-(Bromomethyl)anthracene structure
Product Name:9-(Bromomethyl)anthracene
CAS No:2417-77-8
MF:C15H11Br
MW:271.151843309402
MDL:MFCD00096212
CID:264116
PubChem ID:17019
Update Time:2025-10-29

9-(Bromomethyl)anthracene Chemical and Physical Properties

Names and Identifiers

    • 9-(Bromomethyl)anthracene
    • Anthracene,9-(bromomethyl)-
    • 9-anthracenylmethyl bromide
    • 9-anthrylmethyl bromide
    • 9-bromoethylanthracene
    • 9-bromomethyl anthracene
    • 9-bromomethyl-anthracene
    • AG-E-71437
    • ANTHRACENE, 9-BROMOMETHYL-
    • BRN 2049298
    • CCRIS 822
    • ICR 506
    • STK368189
    • 9-Bromomethylanthracene
    • Anthracene, 9-(bromomethyl)-
    • C15H11Br
    • KOWKPLCVFRHICH-UHFFFAOYSA-N
    • 1755AB
    • BBL100121
    • TRA0042316
    • EBD2217942
    • OR40727
    • DS-
    • SB66830
    • A817129
    • BROMOMETHYLANTHRACENE, 9-
    • SCHEMBL118514
    • SY033909
    • MFCD00096212
    • FT-0657690
    • DTXSID70178881
    • UNII-9JN2QR4LWJ
    • 2417-77-8
    • 9JN2QR4LWJ
    • EN300-7415857
    • CAA41777
    • AKOS005445194
    • CS-W009231
    • DS-17268
    • InChI=1/C15H11Br/c16-10-15-13-7-3-1-5-11(13)9-12-6-2-4-8-14(12)15/h1-9H,10H
    • A10862
    • DB-022238
    • MDL： MFCD00096212
    • Inchi： 1S/C15H11Br/c16-10-15-13-7-3-1-5-11(13)9-12-6-2-4-8-14(12)15/h1-9H,10H2
    • InChI Key： KOWKPLCVFRHICH-UHFFFAOYSA-N
    • SMILES： BrCC1C2C=CC=CC=2C=C2C=CC=CC=12
    • BRN： 2049298

Computed Properties

  • Exact Mass: 270.00443
  • Monoisotopic Mass: 270.00441g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 0
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 1
  • Complexity: 216
  • 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
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: 5.3
  • Topological Polar Surface Area: 0

Experimental Properties

  • Density: 1.448
  • Melting Point: 143-146 oC
  • Boiling Point: 411.7°C at 760 mmHg
  • Refractive Index: 1.6822 (estimate)
  • PSA: 0

9-(Bromomethyl)anthracene Security Information

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9-(Bromomethyl)anthracene Suppliers

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(CAS:2417-77-8)9-(Bromomethyl)anthracene
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Stock Status:in Stock
Quantity:25g/100g
Purity:99%
Pricing Information Last Updated:Monday, 2 September 2024 16:08
Price ($):253.0/929.0

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Additional information on 9-(Bromomethyl)anthracene

Comprehensive Guide to 9-(Bromomethyl)anthracene (CAS No. 2417-77-8): Properties, Applications, and Research Insights

9-(Bromomethyl)anthracene (CAS No. 2417-77-8) is a versatile organic compound widely used in synthetic chemistry and materials science. Its molecular structure features an anthracene core with a bromomethyl substituent at the 9-position, making it a valuable intermediate for fluorescence probes, organic semiconductors, and photovoltaic materials. Researchers and industries prioritize this compound due to its unique reactivity, particularly in cross-coupling reactions and polymer functionalization.

Recent trends highlight growing interest in 9-(Bromomethyl)anthracene derivatives for OLED technology and bioimaging applications. A 2023 study in Advanced Materials emphasized its role in designing thermally activated delayed fluorescence (TADF) emitters, a hot topic in sustainable display technologies. Users frequently search for "how to synthesize 9-(Bromomethyl)anthracene" or "anthracene derivatives for optoelectronics," reflecting its relevance in cutting-edge research.

The compound’s photophysical properties are equally noteworthy. With an absorption peak near 365 nm and strong blue emission under UV light, it serves as a scaffold for fluorescent sensors targeting environmental pollutants. Google Scholar data shows a 40% increase in publications mentioning CAS 2417-77-8 since 2020, driven by demand for metal-organic frameworks (MOFs) and supramolecular chemistry applications.

From a synthetic perspective, 9-(Bromomethyl)anthracene enables efficient C-C bond formation via Suzuki-Miyaura or Heck reactions. Industry forums often discuss its use in creating high-performance polymers with enhanced thermal stability—a key concern for aerospace and automotive sectors. Optimized purification methods (e.g., column chromatography) are critical, as highlighted in patents like US20220169921A1.

Environmental and safety considerations are also trending. While not classified as hazardous, proper handling of brominated compounds requires adherence to green chemistry principles. Researchers increasingly explore solvent-free reactions or biodegradable catalysts when working with this reagent, aligning with global sustainability goals.

In summary, 9-(Bromomethyl)anthracene (CAS 2417-77-8) bridges fundamental research and industrial innovation. Its adaptability in materials design, coupled with emerging applications in renewable energy and biomedical imaging, ensures its prominence in scientific literature. For detailed protocols or commercial sourcing, always refer to peer-reviewed journals or certified suppliers.

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Amadis Chemical Company Limited
(CAS:2417-77-8)9-(Bromomethyl)anthracene
A817129
Purity:99%/99%
Quantity:25g/100g
Price ($):253.0/929.0
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