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Atomfair 3-Bromophenanthrene C14H9Br
Description 3-Bromophenanthrene (CAS No. 62162-97-4) is a high-purity brominated aromatic hydrocarbon with the molecular formula C14H9Br. This compound is a valuable intermediate in organic synthesis, particularly in the construction of polycyclic aromatic hydrocarbons (PAHs) and functionalized phenanthrene derivatives. Its rigid fused-ring structure and bromine substituent make it an ideal precursor for cross-coupling reactions such as Suzuki, Stille, and Heck couplings. Available in >98% purity, this product is rigorously tested via GC-MS and1H NMR to ensure batch-to-batch consistency. Suitable for advanced materials research, pharmaceutical development, and as a building block for organic electronic materials. Packaged under inert gas in amber glass…
Description
Description
3-Bromophenanthrene (CAS No. 62162-97-4) is a high-purity brominated aromatic hydrocarbon with the molecular formula C14H9Br. This compound is a valuable intermediate in organic synthesis, particularly in the construction of polycyclic aromatic hydrocarbons (PAHs) and functionalized phenanthrene derivatives. Its rigid fused-ring structure and bromine substituent make it an ideal precursor for cross-coupling reactions such as Suzuki, Stille, and Heck couplings. Available in >98% purity, this product is rigorously tested via GC-MS and 1H NMR to ensure batch-to-batch consistency. Suitable for advanced materials research, pharmaceutical development, and as a building block for organic electronic materials. Packaged under inert gas in amber glass vials to ensure stability.
- CAS No: 62162-97-4
- Molecular Formula: C14H9Br
- Molecular Weight: 257.12
- Exact Mass: 255.98876
- Monoisotopic Mass: 255.98876
- IUPAC Name: 3-bromophenanthrene
- SMILES: C1=CC=C2C(=C1)C=CC3=C2C=C(C=C3)Br
- Synonyms: 3-Bromophenanthrene, BNGNNFQSUWVWCW-UHFFFAOYSA-, 695-586-3, inchi=1/c14h9br/c15-12-8-7-11-6-5-10-3-1-2-4-13(10)14(11)9-12/h1-9h, 715-50-4
Application
3-Bromophenanthrene serves as a key synthon in materials science for developing organic semiconductors and luminescent materials. Researchers utilize its bromine moiety for palladium-catalyzed cross-coupling reactions to create extended ??-conjugated systems. The compound finds particular use in synthesizing phenanthrene-based ligands for metal-organic frameworks (MOFs) and as a precursor for nonlinear optical materials. Its rigid structure makes it valuable for studying intermolecular interactions in crystal engineering.
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