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Atomfair 4-tert-Butylphenylboronic acid C10H15BO2

Description 4-tert-Butylphenylboronic acid (CAS No. 123324-71-0) is a high-purity boronic acid derivative with the molecular formula C10H15BO2. This organoboron compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its excellent reactivity and stability. The presence of the tert -butyl group enhances its steric and electronic properties, making it a valuable reagent for constructing complex aromatic frameworks. Ideal for pharmaceutical, agrochemical, and materials science research, our product is rigorously tested to ensure ??95% purity (HPLC) and is supplied as a white to off-white crystalline powder. Store in a cool, dry place under inert conditions to maintain…

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Description

Description

4-tert-Butylphenylboronic acid (CAS No. 123324-71-0) is a high-purity boronic acid derivative with the molecular formula C10H15BO2. This organoboron compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its excellent reactivity and stability. The presence of the tert-butyl group enhances its steric and electronic properties, making it a valuable reagent for constructing complex aromatic frameworks. Ideal for pharmaceutical, agrochemical, and materials science research, our product is rigorously tested to ensure ??95% purity (HPLC) and is supplied as a white to off-white crystalline powder. Store in a cool, dry place under inert conditions to maintain optimal stability.

  • CAS No: 123324-71-0
  • Molecular Formula: C10H15BO2
  • Molecular Weight: 178.04
  • Exact Mass: 178.1165099
  • Monoisotopic Mass: 178.1165099
  • IUPAC Name: (4-tert-butylphenyl)boronic acid
  • SMILES: B(C1=CC=C(C=C1)C(C)(C)C)(O)O
  • Synonyms: 4-tert-Butylphenylboronic acid, 123324-71-0, (4-tert-butylphenyl)boronic Acid, DTXSID60370211, DTXCID00321247

Application

4-tert-Butylphenylboronic acid is a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of biaryl compounds for pharmaceuticals and advanced materials. It is also employed in the development of sensors and catalysts due to its boronic acid functionality. Researchers leverage its sterically hindered structure to study steric effects in organic transformations.

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