Atomfair 4-Bromo-4′-pentyl-1,1′-biphenyl C17H19Br CAS 63619-59-0

Description

4-Bromo-4′-pentyl-1,1′-biphenyl (CAS No. 63619-59-0) is a high-purity organic compound with the molecular formula C₁₇H₁₉Br. This biphenyl derivative features a bromine substituent at the 4-position and a pentyl chain at the 4′-position, offering unique reactivity and structural properties. It is commonly utilized in advanced organic synthesis, liquid crystal research, and material science applications. The compound is supplied as a crystalline solid with ≥98% purity (HPLC), ensuring consistency for sensitive research applications. Proper storage under inert conditions is recommended to maintain stability.

Properties

• CAS Number: 63619-59-0
• Complexity: 210
• IUPAC Name: 1-bromo-4-(4-pentylphenyl)benzene
• InChI: InChI=1S/C17H19Br/c1-2-3-4-5-14-6-8-15(9-7-14)16-10-12-17(18)13-11-16/h6-13H,2-5H2,1H3
• InChI Key: VXJTWTJULLKDPY-UHFFFAOYSA-N
• Exact Mass: 302.06701
• Molecular Formula: C17H19Br
• Molecular Weight: 303.2
• SMILES: CCCCCC1=CC=C(C=C1)C2=CC=C(C=C2)Br
• Monoisotopic Mass: 302.06701
• Synonyms: 63619-59-0, 4-Bromo-4′-pentylbiphenyl, 4-Bromo-4′-pentyl-1,1′-biphenyl, 4-Bromo-4′-n-pentylbiphenyl, 1-bromo-4-(4-pentylphenyl)benzene, MFCD00060106, Maybridge1_002125, 4-Amyl-4′-bromobiphenyl, 1,1′-Biphenyl, 4-bromo-4′-pentyl-, 4-Bromo-4-N-Pentylbiphenyl, 4-pentyl4′-bromobiphenyl, 4-bromo-4′-pentyl-biphenyl, 4′-Bromo-4-pentyl-biphenyl, 4-Bromo-4′-n-pentylbiohenyl, SCHEMBL1599747, SCHEMBL27900187, HMS547I13, DTXSID60347185, 1-(4-bromophenyl)-4-pentylbenzene, AKOS015835673, 1,1′-Biphenyl-4-bromo-4′-n-pentyl, CS-W009946, 4-Bromo-4′-pentyl-1,1′-biphenyl #, DS-18298, SY038328, B1305, F16575, 4-Bromo-4 inverted exclamation mark -pentylbiphenyl

Application

4-Bromo-4′-pentyl-1,1′-biphenyl serves as a key intermediate in the synthesis of liquid crystalline materials for display technologies. Researchers employ it in Suzuki coupling reactions to create extended π-conjugated systems for organic electronics. Its structural motif is also valuable in pharmaceutical research for building biphenyl-based scaffolds.

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