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CAS 480438-57-1

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3-Chloro-4-propoxyphenylboronic acid

Description:
3-Chloro-4-propoxyphenylboronic 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, particularly in organic synthesis and medicinal chemistry. The compound features a chlorinated aromatic ring, which can influence its reactivity and solubility. The propoxy group enhances its lipophilicity, potentially improving its bioavailability in pharmaceutical contexts. This compound is typically utilized in Suzuki-Miyaura cross-coupling reactions, a key method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, the presence of the boronic acid moiety allows for the formation of boronate esters, which can be further manipulated in synthetic pathways. Its unique structural features make it a valuable intermediate in the development of various biologically active compounds. As with many boronic acids, it is important to handle this substance with care, as it may exhibit sensitivity to moisture and air, which can affect its stability and reactivity.
Formula:C9H12BClO3
InChI:InChI=1/C9H12BClO3/c1-2-5-14-9-4-3-7(10(12)13)6-8(9)11/h3-4,6,12-13H,2,5H2,1H3
SMILES:CCCOc1ccc(cc1Cl)B(O)O
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