Description

9-Bromo-10-(naphthalen-1-yl)anthracene (CAS No. 400607-04-7) is a high-purity organic compound with the molecular formula C₂₄H₁₅Br. This brominated anthracene derivative features a naphthalene substituent at the 10-position, making it a valuable intermediate in organic synthesis and materials science. With a molecular weight of 383.28 g/mol, this compound exhibits excellent thermal stability and is commonly used in the development of organic semiconductors, OLEDs, and photoluminescent materials. Its rigid polycyclic structure and bromine functionality allow for further functionalization via cross-coupling reactions, such as Suzuki or Stille couplings. Ideal for researchers in optoelectronics and advanced material design, this product is available in >98% purity (HPLC) and is supplied in carefully sealed packaging to ensure stability and longevity.

Properties

• CAS Number: 400607-04-7
• Complexity: 435
• IUPAC Name: 9-bromo-10-(1-naphthyl)anthracene
• InChI: InChI=1S/C24H15Br/c25-24-21-13-5-3-11-19(21)23(20-12-4-6-14-22(20)24)18-15-7-9-16-8-1-2-10-17(16)18/h1-15H
• InChI Key: SYACRXBYRNYMLN-UHFFFAOYSA-N
• Exact Mass: 382.03571
• Molecular Formula: C24H15Br
• Molecular Weight: 383.3
• SMILES: C1=CC=C2C(=C1)C=CC=C2C3=C4C=CC=CC4=C(C5=CC=CC=C53)Br
• Monoisotopic Mass: 382.03571
• Synonyms: 400607-04-7, 9-bromo-10-(naphthalen-1-yl)anthracene, 9-bromo-10-(1-naphthyl)anthracene, 9-Bromo-10-(1-naphthalenyl)anthracene, Anthracene, 9-bromo-10-(1-naphthalenyl)-, MFCD11046571, 9-bromo-10-naphthalen-1-ylanthracene, 9-bromo-10-(1-naphthalenyl)-anthracene, Anthracene, 9-bromo-10-(1-naphthalenyl), SCHEMBL1680196, DTXSID90610576, AKOS015835052, AC-5806, AC-24828, AS-19012, SY032217, B4451, CS-0097275, 9-Bromo-10-(naphthalen-1-yl)anthraceneSuppliers

Application

9-Bromo-10-(naphthalen-1-yl)anthracene is widely utilized as a key building block in the synthesis of organic electronic materials, particularly for OLEDs and photovoltaic devices. Its extended π-conjugation system enhances charge transport properties, making it suitable for light-emitting layers in display technologies. Researchers also employ this compound in the development of fluorescent probes and sensors due to its strong photoluminescence. Additionally, it serves as a precursor for polymerization reactions to create conjugated polymers with tailored optoelectronic characteristics.

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