Description
9-Bromo-10-(2-naphthyl)anthracene (CAS No. 474688-73-8) is a high-purity organic compound with the molecular formula C24H15Br. This brominated anthracene derivative features a naphthyl substituent at the 10-position, making it a valuable building block for advanced organic synthesis and materials science research. With an IUPAC name of 9-bromo-10-naphthalen-2-ylanthracene, this compound is characterized by its extended π-conjugated system, which is ideal for studies in optoelectronics, organic semiconductors, and fluorescent materials. Our product is rigorously tested to ensure ≥95% purity (HPLC) and is supplied as a crystalline solid with detailed spectral data (NMR, MS) for verification. Suitable for use in Suzuki couplings, cross-coupling reactions, and as a precursor for polycyclic aromatic hydrocarbon (PAH) frameworks. Packaged under inert gas to ensure stability and shipped with a Certificate of Analysis.
Properties
- CAS Number: 474688-73-8
- Complexity: 435
- IUPAC Name: 9-bromo-10-(2-naphthyl)anthracene
- InChI: InChI=1S/C24H15Br/c25-24-21-11-5-3-9-19(21)23(20-10-4-6-12-22(20)24)18-14-13-16-7-1-2-8-17(16)15-18/h1-15H
- InChI Key: FKIFDWYMWOJKTQ-UHFFFAOYSA-N
- Exact Mass: 382.03571
- Molecular Formula: C24H15Br
- Molecular Weight: 383.3
- SMILES: C1=CC=C2C=C(C=CC2=C1)C3=C4C=CC=CC4=C(C5=CC=CC=C53)Br
- Monoisotopic Mass: 382.03571
- Synonyms: 9-bromo-10-(2-naphthyl)anthracene, 474688-73-8, 9-bromo-10-(naphthalen-2-yl)anthracene, MFCD09832882, 9-bromo-10-(2-naphthyl)-anthracene, 9-bromo-10-naphthalen-2-ylanthracene, 9-Bromo-10-(2-naphthyl) anthracene, 9-bromo-10-(naphthalen-2-yl)anthracen, 10-bromo-9-(naphthalen-2-yl)anthracene, Anthracene, 9-bromo-10-(2-naphthalenyl)-, SCHEMBL169491, DTXSID20583042, BCP28647, AKOS015896001, SB66491, 9-bromo-10-(2-naphthalenyl)Anthracene, 9-bromo-10-(naphthalene-2-yl)anthracene, AS-39325, SY037140, 9-bromo-10-(naphthalen-2-yl) anthracene, 9-bromo-10-(naphthalene-2-yl) anthracene, B4426, CS-0159977
Application
9-Bromo-10-(2-naphthyl)anthracene is widely used in the development of organic light-emitting diodes (OLEDs) due to its efficient luminescence and charge transport properties. Researchers employ this compound as a key intermediate in the synthesis of conjugated polymers for photovoltaic devices. Its rigid anthracene-naphthyl structure also makes it a candidate for studying aggregation-induced emission (AIE) phenomena in material science.
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