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CAS 175883-60-0

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3-CHLORO-4-METHOXYPHENYLBORONIC ACID

Description:
3-Chloro-4-methoxyphenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that has both a chlorine and a methoxy substituent. This compound typically appears as a white to off-white solid and is soluble in polar organic solvents. The chlorine atom introduces a halogen functionality, which can enhance reactivity in cross-coupling reactions, while the methoxy group can influence the electronic properties of the aromatic ring, making it more nucleophilic. Boronic acids are known for their ability to form reversible complexes with diols, which is significant in various applications, including organic synthesis and medicinal chemistry. This compound is often utilized in Suzuki-Miyaura coupling reactions, a key method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, its unique structural features may contribute to its potential use in pharmaceuticals and agrochemicals, where selective reactivity and functionalization are essential. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C7H8BClO3
InChI:InChI=1/C8H10BClO3/c1-2-13-8-4-3-6(9(11)12)5-7(8)10/h3-5,11-12H,2H2,1H3
SMILES:CCOc1ccc(cc1Cl)B(O)O
Synonyms:
  • Akos Brn-0653
  • 3-Chloro-4-Methoxybenzeneboronic Acid
  • (3-Chloro-4-Ethoxyphenyl)Boronic Acid
  • 3-CHLORO-4-METHOXYPHENYLBORONIC ACID
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