4-(4′-(2-Pentyloxy)phenyl)phenylboronic acid(contains varying amounts of Anhydride)

98%

Reagent Code: #227462
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CAS Number 1072951-79-1

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Weight 284.16 g/mol
Formula C₁₇H₂₁BO₃
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MDL Number MFCD09038419
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Storage Room temperature

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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. Its boronic acid functionality enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of liquid crystals, organic semiconductors, and bioactive compounds. The presence of the pentyloxyphenyl group enhances solubility and electronic properties, which can influence the performance of materials in optoelectronic devices. Commonly employed in research and development for constructing biaryl structures in drug discovery and functional materials.

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inventory 1g
10-20 days ฿5,630.00

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4-(4′-(2-Pentyloxy)phenyl)phenylboronic acid(contains varying amounts of Anhydride)
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. Its boronic acid functionality enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of liquid crystals, organic semiconductors, and bioactive compounds. The presence of the pentyloxyphenyl group enhances solubility and electronic properties, which can influence the performanc

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. Its boronic acid functionality enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of liquid crystals, organic semiconductors, and bioactive compounds. The presence of the pentyloxyphenyl group enhances solubility and electronic properties, which can influence the performance of materials in optoelectronic devices. Commonly employed in research and development for constructing biaryl structures in drug discovery and functional materials.

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