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CAS 603122-82-3

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[3-chloro-4-(methoxycarbonyl)phenyl]boronic acid

Description:
[3-Chloro-4-(methoxycarbonyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a chloro substituent and a methoxycarbonyl group on a phenyl ring, contributing to its reactivity and solubility properties. Typically, boronic acids are polar and can participate in Suzuki coupling reactions, which are valuable in forming carbon-carbon bonds. This specific compound may exhibit moderate solubility in polar organic solvents and can be sensitive to moisture due to the presence of the boronic acid group. Its structure suggests potential applications in drug development and materials science, particularly in the synthesis of complex organic molecules. Additionally, the presence of the methoxycarbonyl group may enhance its stability and influence its electronic properties, making it a versatile building block in synthetic chemistry.
Formula:C8H8BClO4
InChI:InChI=1/C8H8BClO4/c1-14-8(11)6-3-2-5(9(12)13)4-7(6)10/h2-4,12-13H,1H3
SMILES:COC(=O)c1ccc(cc1Cl)B(O)O
Synonyms:
  • (3-Chloro-4-(methoxycarbonyl)phenyl)boronicacid
  • 3-Chloro-4-(methoxycarbonyl)phenylboronic acid
  • (3-Chloro-4-Methoxycarbonyl)Benzeneboronic Acid
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