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Atomfair (4-pentylphenyl)boronic Acid 4-Pentylphenylboronic Acid C11H17BO2

Description (4-Pentylphenyl)boronic Acid (CAS No. 121219-12-3) is a high-purity boronic acid derivative with the molecular formula C11H17BO2. This organoboron compound features a pentylphenyl group attached to a boronic acid functional group, making it a versatile intermediate in synthetic organic chemistry and materials science. With a molecular weight of 192.06 g/mol, it is commonly utilized in Suzuki-Miyaura cross-coupling reactions, a cornerstone methodology for C-C bond formation in pharmaceutical and agrochemical research. The compound is supplied as a white to off-white crystalline powder, ensuring consistent reactivity and performance. Store under inert conditions to maintain stability, as boronic acids are sensitive to moisture…

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Description

Description

(4-Pentylphenyl)boronic Acid (CAS No. 121219-12-3) is a high-purity boronic acid derivative with the molecular formula C11H17BO2. This organoboron compound features a pentylphenyl group attached to a boronic acid functional group, making it a versatile intermediate in synthetic organic chemistry and materials science. With a molecular weight of 192.06 g/mol, it is commonly utilized in Suzuki-Miyaura cross-coupling reactions, a cornerstone methodology for C-C bond formation in pharmaceutical and agrochemical research. The compound is supplied as a white to off-white crystalline powder, ensuring consistent reactivity and performance. Store under inert conditions to maintain stability, as boronic acids are sensitive to moisture and oxidation. Ideal for researchers requiring precise functionalization of aromatic systems.

  • CAS No: 121219-12-3
  • Molecular Formula: C11H17BO2
  • Molecular Weight: 192.06
  • Exact Mass: 192.1321599
  • Monoisotopic Mass: 192.1321599
  • IUPAC Name: (4-pentylphenyl)boronic acid
  • SMILES: B(C1=CC=C(C=C1)CCCCC)(O)O
  • Synonyms: 121219-12-3, (4-pentylphenyl)boronic Acid, 4-n-Pentylphenylboronic acid, 4-Pentylphenylboronic Acid, 4-Pentylbenzeneboronic acid

Application

(4-Pentylphenyl)boronic Acid is widely employed in palladium-catalyzed cross-coupling reactions, particularly Suzuki-Miyaura couplings, to synthesize biaryl structures prevalent in drug discovery. It serves as a key building block for liquid crystal materials due to its mesogenic pentylphenyl moiety. Researchers also use it to modify organic semiconductors and metal-organic frameworks (MOFs) for advanced material applications.

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