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CAS 219735-99-6

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(2-Chloro-4-methoxyphenyl)boronic acid

Description:
(2-Chloro-4-methoxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with a chlorine atom and a methoxy group. This compound typically appears as a white to off-white solid and is soluble in polar organic solvents. It is known for its utility in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are pivotal for forming carbon-carbon bonds. The presence of the boronic acid group allows for the formation of stable complexes with diols, making it useful in various applications, including drug discovery and materials science. Additionally, the chlorine and methoxy substituents can influence the electronic properties and reactivity of the compound, enhancing its role in medicinal chemistry. Safety precautions should be taken when handling this compound, as boronic acids can be sensitive to moisture and may require specific storage conditions to maintain stability.
Formula:C7H8BClO3
InChI:InChI=1/C7H8BClO3/c1-12-7-4-5(9)2-3-6(7)8(10)11/h2-4,10-11H,1H3
SMILES:COc1cc(ccc1B(O)O)Cl
Synonyms:
  • 2-Chloro-4-methoxyphenylboronicacid
  • (4-Chloro-2-Methoxyphenyl)Boronic Acid
  • 2-Chloro-4-Methoxybenzeneboronic Acid
  • 2-Chloro-4-methoxyphenylboronic acid
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