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CAS 156641-98-4

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6-Methoxy-2-naphthaleneboronic acid

Description:
6-Methoxy-2-naphthaleneboronic acid is an organic compound characterized by the presence of a boronic acid functional group attached to a naphthalene ring that is further substituted with a methoxy group. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar organic solvents. The boronic acid moiety allows for the formation of reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. Its methoxy substituent can influence the compound's electronic properties and reactivity, enhancing its utility in cross-coupling reactions, such as Suzuki-Miyaura coupling. Additionally, 6-Methoxy-2-naphthaleneboronic acid may exhibit biological activity, making it a candidate for further research in drug development. Safety data should be consulted for handling and storage, as boronic acids can be sensitive to moisture and may require specific precautions. Overall, this compound serves as a valuable building block in the synthesis of complex organic molecules.
Formula:C12H13BO3
InChI:InChI=1/C12H13BO3/c1-2-16-12-6-4-9-7-11(13(14)15)5-3-10(9)8-12/h3-8,14-15H,2H2,1H3
SMILES:CCOc1ccc2cc(ccc2c1)B(O)O
Synonyms:
  • 6-Methoxy-2-naphthylboronic acid
  • (6-Methoxynaphthalen-2-Yl)Boronic Acid
  • (6-Ethoxynaphthalen-2-Yl)Boronic Acid
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