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CAS 156642-03-4

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4'-METHOXYBIPHENYLBORONIC ACID

Description:
4'-Methoxyboronic acid, with the CAS number 156642-03-4, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a biphenyl structure, specifically with a methoxy substituent at the para position of one of the phenyl rings. This compound typically appears as a white to off-white solid and is soluble in polar organic solvents. It exhibits properties typical of boronic acids, such as the ability to form reversible complexes with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The methoxy group enhances its solubility and reactivity, allowing it to participate in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is pivotal in the formation of carbon-carbon bonds. Additionally, 4'-methoxyboronic acid can serve as a building block in the synthesis of more complex organic molecules, including pharmaceuticals and agrochemicals, due to its versatile reactivity and functionalization potential.
Formula:C13H13BO3
InChI:InChI=1/C13H13BO3/c1-17-13-8-4-11(5-9-13)10-2-6-12(7-3-10)14(15)16/h2-9,15-16H,1H3
SMILES:COc1ccc(cc1)c1ccc(cc1)B(O)O
Synonyms:
  • Akos Brn-0081
  • 4-(4-Methoxyphenyl)Phenylboronic Acid
  • 4'-Methoxy-4-Biphenylboronic Acid
  • 4'-Methoxybiphenyl-4-Ylboronic Acid
  • 4-(4-Methoxyphenyl)benzeneboronic acid
  • 4'-Methoxybiphenyl-4-boronic acid
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