Atomfair 1-Bromo-8-phenylnaphthalene C16H11Br

Description 1-Bromo-8-phenylnaphthalene (CAS No. 1121545-24-1) is a high-purity aromatic brominated compound with the molecular formula C16H11Br . This specialized organic intermediate features a naphthalene core substituted with a bromine atom at the 1-position and a phenyl group at the 8-position, offering unique steric and electronic properties for advanced synthetic applications. Ideal for researchers in materials science and pharmaceutical chemistry, this compound is characterized by its excellent stability and reactivity in cross-coupling reactions (e.g., Suzuki, Stille). Available in rigorously controlled batches with ??95% purity (GC), it is supplied in amber glass vials under inert atmosphere to ensure long-term integrity. NMR, HPLC,…

Description

Description

1-Bromo-8-phenylnaphthalene (CAS No. 1121545-24-1) is a high-purity aromatic brominated compound with the molecular formula C16H11Br. This specialized organic intermediate features a naphthalene core substituted with a bromine atom at the 1-position and a phenyl group at the 8-position, offering unique steric and electronic properties for advanced synthetic applications. Ideal for researchers in materials science and pharmaceutical chemistry, this compound is characterized by its excellent stability and reactivity in cross-coupling reactions (e.g., Suzuki, Stille). Available in rigorously controlled batches with ??95% purity (GC), it is supplied in amber glass vials under inert atmosphere to ensure long-term integrity. NMR, HPLC, and MS data are provided for quality verification.

  • CAS No: 1121545-24-1
  • Molecular Formula: C16H11Br
  • Molecular Weight: 283.16
  • Exact Mass: 282.00441
  • Monoisotopic Mass: 282.00441
  • IUPAC Name: 1-bromo-8-phenylnaphthalene
  • SMILES: C1=CC=C(C=C1)C2=CC=CC3=C2C(=CC=C3)Br
  • Synonyms: 1-Bromo-8-phenylnaphthalene, 1121545-24-1, 1-bromo-8phenylnaphthalene, 1-Bromo-8-phenyl-naphthalene, SCHEMBL15457919

Application

1-Bromo-8-phenylnaphthalene serves as a key building block in the synthesis of polycyclic aromatic hydrocarbons (PAHs) for organic semiconductors and OLED materials. Its sterically hindered structure facilitates studies on ??-conjugation extension in optoelectronic materials. The compound is also employed in pharmaceutical research for creating constrained biaryl motifs in drug discovery. Researchers utilize it in palladium-catalyzed cross-coupling reactions to construct complex aromatic architectures.

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