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CAS 870778-88-4

:

[2-methoxy-6-(1-methylethoxy)phenyl]boronic acid

Description:
[2-Methoxy-6-(1-methylethoxy)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. This compound features a phenyl ring substituted with a methoxy group and an ethoxy group, enhancing its solubility and reactivity. The boronic acid moiety allows for participation in various chemical reactions, including Suzuki coupling, which is significant in organic synthesis and materials science. The presence of the methoxy and ethoxy groups can influence the electronic properties of the molecule, potentially affecting its reactivity and interaction with other chemical species. Additionally, boronic acids are often utilized in medicinal chemistry for their ability to interact with biological targets, making this compound of interest in drug development. Its stability, solubility in organic solvents, and reactivity with nucleophiles are key characteristics that define its utility in synthetic applications.
Formula:C10H15BO4
InChI:InChI=1/C10H15BO4/c1-7(2)15-9-6-4-5-8(14-3)10(9)11(12)13/h4-7,12-13H,1-3H3
SMILES:CC(C)Oc1cccc(c1B(O)O)OC
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