Description

1-(4′-Bromo-biphenyl-4-yl)-propan-1-one (CAS No. 58743-84-3) is a high-purity brominated aromatic ketone with the molecular formula C₁₅H₁₃BrO. This compound, also known by its IUPAC name 1-[4-(4-bromophenyl)phenyl]propan-1-one, is a valuable intermediate in organic synthesis and materials science. It features a biphenyl core functionalized with a propan-1-one group and a bromine substituent, making it highly versatile for cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions. The product is rigorously tested for purity and stability, ensuring optimal performance in research and industrial applications. Available in various quantities, it is supplied with comprehensive analytical data (including HPLC, NMR, and MS) to meet the stringent requirements of pharmaceutical, agrochemical, and advanced materials research.

Properties

• CAS Number: 58743-84-3
• Complexity: 248
• IUPAC Name: 1-[4-(4-bromophenyl)phenyl]propan-1-one
• InChI: InChI=1S/C15H13BrO/c1-2-15(17)13-5-3-11(4-6-13)12-7-9-14(16)10-8-12/h3-10H,2H2,1H3
• InChI Key: ULSVFFKCSNLWNU-UHFFFAOYSA-N
• Exact Mass: 288.01498
• Molecular Formula: C15H13BrO
• Molecular Weight: 289.17
• SMILES: CCC(=O)C1=CC=C(C=C1)C2=CC=C(C=C2)Br
• Topological: 17.1
• Monoisotopic Mass: 288.01498
• Synonyms: SCHEMBL8987897, MFCD19386932, AKOS013203624, 58743-84-3, 1-(4′-Bromo-biphenyl-4-yl)-propan-1-one, 1-(4′-Bromo-[1,1′-biphenyl]-4-yl)propan-1-one

Application

1-(4′-Bromo-biphenyl-4-yl)-propan-1-one is widely used as a key intermediate in the synthesis of advanced organic materials and pharmaceuticals. Its bromine moiety enables participation in palladium-catalyzed cross-coupling reactions, facilitating the construction of complex biaryl systems. Researchers utilize this compound in the development of liquid crystals, OLED materials, and bioactive molecules. It is also employed in agrochemical research for the design of novel pesticides and herbicides.

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