2-(4-Bromophenyl)-1-phenylnaphthalene丨CAS 1533415-48-3

2-(4-Bromophenyl)-1-phenylnaphthalene丨CAS 1533415-48-3
Product Introduction:
Catalog No.: SS069517
CAS No.: 1533415-48-3
Purity: 98%min
Product Name: 2-(4-Bromophenyl)-1-phenylnaphthalene
Molecular Formula: C22H15Br
Molecular Weight: 359.3
Synonym(s): Naphthalene, 2-(4-bromophenyl)-1-phenyl-
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Technical Parameters
Description

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Specifications

 

Appearance White solid
Purity 98% min

 

 

 

Applications

 

2-(4-Bromophenyl)-1-phenylnaphthalene (CAS 1533415-48-3) is a brominated polycyclic aromatic compound used primarily as an intermediate in organic synthesis, materials science, and medicinal chemistry. Its bromophenyl and naphthalene moieties make it suitable for cross-coupling reactions such as Suzuki, Heck, and Sonogashira couplings, enabling the construction of larger π-conjugated systems. In materials research, it is applied in the synthesis of organic semiconductors, light-emitting materials, and photonic devices due to its rigid aromatic structure and extended conjugation. In medicinal chemistry, it can serve as a building block for designing bioactive molecules and molecular probes where planar aromatic frameworks enhance stacking interactions and binding affinity.

 

Benefits

 

The benefits of 2-(4-bromophenyl)-1-phenylnaphthalene lie in its chemical versatility, structural rigidity, and electronic properties. The bromine atom acts as a reactive site for selective substitution and cross-coupling, allowing precise functionalization. Its fused naphthalene and phenyl system provides a stable, planar aromatic core that contributes to π–π interactions, thermal stability, and electronic delocalization in materials and molecular design. The combination of reactivity and structural stability makes it a valuable intermediate for constructing complex aromatic frameworks, facilitating efficient synthesis of advanced materials and bioactive compounds.

 

Conclusion

 

In summary, 2-(4-bromophenyl)-1-phenylnaphthalene is a multifunctional intermediate used in organic synthesis, materials science, and medicinal chemistry. Its applications include cross-coupling reactions, organic semiconductors, and bioactive molecule design, while its benefits come from selective reactivity, rigid planar structure, and favorable electronic properties. With these characteristics, it remains a key building block for developing high-performance materials and complex aromatic compounds.

 

 

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