Description

1-Bromo-4-phenylnaphthalene (CAS No. 59951-65-4) is a high-purity organic compound with the molecular formula C₁₆H₁₁Br, designed for advanced research and industrial applications. This aromatic brominated naphthalene derivative is characterized by its phenyl substitution at the 4-position, making it a valuable intermediate in synthetic organic chemistry, materials science, and pharmaceutical development. The compound is supplied as a crystalline solid with exceptional purity (>98%) and is rigorously tested to meet the stringent demands of researchers and scientists. Ideal for use in cross-coupling reactions, Suzuki-Miyaura couplings, and as a building block for fluorescent materials or liquid crystals. Packaged under inert conditions to ensure stability and longevity.

Properties

• CAS Number: 59951-65-4
• Complexity: 244
• IUPAC Name: 1-bromo-4-phenyl-naphthalene
• InChI: InChI=1S/C16H11Br/c17-16-11-10-13(12-6-2-1-3-7-12)14-8-4-5-9-15(14)16/h1-11H
• InChI Key: ZARGVWJSXZDKRE-UHFFFAOYSA-N
• Exact Mass: 282.00441
• Molecular Formula: C16H11Br
• Molecular Weight: 283.16
• SMILES: C1=CC=C(C=C1)C2=CC=C(C3=CC=CC=C32)Br
• Monoisotopic Mass: 282.00441
• Synonyms: 1-Bromo-4-phenylnaphthalene, 59951-65-4, MFCD17012346, 1-BROMO-4-PHENYL-NAPHTHALENE, Naphthalene, 1-bromo-4-phenyl-, 1-bromo-4-phenyl naphthalene, SCHEMBL2162977, SCHEMBL21410382, DTXSID40483616, CX1337, AKOS016000224, SB67070, AS-19357, SY034409, DB-072731, B5105, CS-0038902

1-Bromo-4-phenylnaphthalene serves as a versatile intermediate in organic synthesis, particularly in palladium-catalyzed cross-coupling reactions for constructing complex aromatic systems. Its phenyl-naphthalene scaffold is useful in materials science for developing optoelectronic materials and liquid crystals. Researchers also employ it in medicinal chemistry for the synthesis of bioactive molecules or fluorescent probes.

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