Cas no 400607-05-8 (9-(1,1'-Biphenyl-4-yl)-10-bromoanthracene)

9-(1,1'-Biphenyl-4-yl)-10-bromoanthracene is a brominated anthracene derivative featuring a biphenyl substituent at the 9-position. This compound is of interest in organic electronics and materials science due to its extended π-conjugation and structural rigidity, which enhance charge transport properties. The bromine atom at the 10-position provides a reactive site for further functionalization, making it a versatile intermediate in the synthesis of advanced organic semiconductors, OLED materials, or liquid crystals. Its well-defined molecular structure and high purity make it suitable for research and development in optoelectronic applications. The compound exhibits good thermal stability and is often utilized in studies exploring structure-property relationships in conjugated systems.
9-(1,1'-Biphenyl-4-yl)-10-bromoanthracene structure
400607-05-8 structure
Product Name:9-(1,1'-Biphenyl-4-yl)-10-bromoanthracene
CAS No:400607-05-8
MF:C26H17Br
MW:409.317186117172
MDL:MFCD19440858
CID:845044
PubChem ID:253662190
Update Time:2025-05-20

9-(1,1'-Biphenyl-4-yl)-10-bromoanthracene Chemical and Physical Properties

Names and Identifiers

    • 9-([1,1'-Biphenyl]-4-yl)-10-bromoanthracene
    • 9-(4-Biphenylyl)-10-bromoanthracene
    • 9-[1,1'-biphenyl]-4-yl-10-bromo-anthracene
    • 9-(4-biphenyl)-10-bromoanthracene
    • 9-(biphenyl-4-yl)-10-bromoanthracene
    • VCJIOUBBOCVHPE-UHFFFAOYSA-N
    • 5300AB
    • OR52350
    • AX8235667
    • 9-(1,1'-Biphenyl-4-yl)-10-bromoanthracene
    • MDL： MFCD19440858
    • Inchi： 1S/C26H17Br/c27-26-23-12-6-4-10-21(23)25(22-11-5-7-13-24(22)26)20-16-14-19(15-17-20)18-8-2-1-3-9-18/h1-17H
    • InChI Key： VCJIOUBBOCVHPE-UHFFFAOYSA-N
    • SMILES： BrC1C2C=CC=CC=2C(C2C=CC(C3C=CC=CC=3)=CC=2)=C2C=CC=CC2=1

Computed Properties

  • Exact Mass: 408.05100
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 0
  • Heavy Atom Count: 27
  • Rotatable Bond Count: 2
  • Complexity: 449
  • Topological Polar Surface Area: 0

Experimental Properties

  • Density: 1.344
  • Melting Point: 251.0 to 255.0 deg-C
  • PSA: 0.00000
  • LogP: 8.08950

9-(1,1'-Biphenyl-4-yl)-10-bromoanthracene Customs Data

  • HS CODE：2903999090
  • Customs Data：

    China Customs Code:

    2903999090

    Overview:

    2903999090 Other aromatic halogenated derivatives. VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:5.5% general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2903999090 halogenated derivatives of aromatic hydrocarbons VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

9-(1,1'-Biphenyl-4-yl)-10-bromoanthracene Pricemore >>

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abcr
AB403543-1 g
9-(4-Biphenylyl)-10-bromoanthracene; .
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abcr
AB403543-5 g
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TRC
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9-(1,1'-Biphenyl-4-yl)-10-bromoanthracene Production Method

9-(1,1'-Biphenyl-4-yl)-10-bromoanthracene Suppliers

Suzhou Senfeida Chemical Co., Ltd
Gold Member
Audited Supplier Audited Supplier
(CAS:400607-05-8)9-[1,1'-biphenyl]-4-yl-10-bromo-anthracene
Order Number:sfd16181
Stock Status:in Stock
Quantity:200kg
Purity:99.9%
Pricing Information Last Updated:Friday, 19 July 2024 14:37
Price ($):discuss personally

9-(1,1'-Biphenyl-4-yl)-10-bromoanthracene Related Literature

Additional information on 9-(1,1'-Biphenyl-4-yl)-10-bromoanthracene

Introduction to 9-(1,1'-Biphenyl-4-yl)-10-bromoanthracene (CAS No. 400607-05-8)

9-(1,1'-Biphenyl-4-yl)-10-bromoanthracene, identified by the Chemical Abstracts Service Number (CAS No.) 400607-05-8, is a sophisticated organic compound that has garnered significant attention in the field of pharmaceutical chemistry and materials science. This compound belongs to the anthracene family, a class of polycyclic aromatic hydrocarbons (PAHs) known for their unique structural and electronic properties. The presence of a bromine substituent at the 10-position and a biphenyl moiety at the 9-position introduces distinct reactivity and functionality, making it a valuable intermediate in synthetic chemistry and a potential candidate for various applications.

The molecular structure of 9-(1,1'-Biphenyl-4-yl)-10-bromoanthracene consists of an anthracene core substituted with a bromine atom at the 10-position and a biphenyl group linked at the 9-position. This arrangement imparts specific electronic and steric properties that are highly relevant for its utility in chemical synthesis and material science. The bromine atom, in particular, serves as a versatile handle for further functionalization, enabling the construction of more complex molecules through cross-coupling reactions such as Suzuki-Miyaura or Buchwald-Hartwig couplings.

In recent years, 9-(1,1'-Biphenyl-4-yl)-10-bromoanthracene has been explored in the development of advanced materials, including organic semiconductors and light-emitting diodes (OLEDs). The anthracene core is renowned for its excellent electron transport properties, while the biphenyl group enhances planarity and conjugation, crucial for efficient charge mobility. The bromine substituent further facilitates post-synthetic modifications, allowing researchers to tailor the compound's properties for specific applications.

One of the most compelling aspects of 9-(1,1'-Biphenyl-4-yl)-10-bromoanthracene is its potential in pharmaceutical research. Anthracene derivatives have a long history of investigation due to their biological activity and structural similarity to naturally occurring PAHs. The introduction of functional groups like bromine can modulate bioactivity, making this compound a promising scaffold for drug discovery. Current studies are focusing on its role as a precursor in synthesizing novel therapeutic agents targeting various diseases.

The synthesis of 9-(1,1'-Biphenyl-4-yl)-10-bromoanthracene typically involves multi-step organic reactions starting from commercially available precursors. A common approach includes the bromination of anthracene followed by coupling with 4-bromobiphenyl using palladium-catalyzed cross-coupling reactions. These synthetic strategies highlight the compound's accessibility and versatility, enabling researchers to explore its full potential.

Recent advancements in computational chemistry have also shed light on the electronic properties of 9-(1,1'-Biphenyl-4-yl)-10-bromoanthracene. Density Functional Theory (DFT) calculations indicate that the presence of the biphenyl group significantly influences the energy levels and electron distribution within the molecule. This information is crucial for designing materials with optimized optoelectronic characteristics, such as those used in flexible electronics and photovoltaic devices.

In addition to its applications in materials science and pharmaceuticals, 9-(1,1'-Biphenyl-4-yl)-10-bromoanthracene has been investigated for its photophysical properties. Anthracene derivatives are known for their strong fluorescence emissions, which make them useful in sensors and bioimaging applications. The bromine substituent can fine-tune these emission properties, offering opportunities to develop highly sensitive detection methods.

The industrial relevance of 9-(1,1'-Biphenyl-4-yl)-10-bromoanthracene is further underscored by its role in developing high-performance polymers. By incorporating this compound into polymer backbones, researchers can achieve enhanced thermal stability and mechanical strength. These attributes are particularly valuable in aerospace and automotive industries where lightweight yet durable materials are essential.

Future research directions for 9-(1,1'-Biphenyl-4-yl)-10-bromoanthracene include exploring its behavior in solution-processable systems and its compatibility with other functional materials. The ability to integrate this compound into diverse chemical frameworks suggests broad applicability across multiple disciplines. As synthetic methodologies continue to evolve, new derivatives and applications are likely to emerge.

In conclusion,9-(1,1'-Biphenyl-4-yl)-10-bromoanthracene (CAS No. 400607-05-8) is a multifaceted compound with significant potential in pharmaceuticals、materials science，and advanced technologies。 Its unique structural features，combined with its synthetic accessibility，make it an indispensable tool for researchers seeking innovative solutions across various scientific domains。

400607-05-8 (9-(1,1'-Biphenyl-4-yl)-10-bromoanthracene) Related Products

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Suzhou Senfeida Chemical Co., Ltd
(CAS:400607-05-8)9-[1,1'-biphenyl]-4-yl-10-bromo-anthracene
sfd16181
Purity:99.9%
Quantity:200kg
Price ($):Inquiry
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