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CAS 352534-84-0

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[3-bromo-5-fluoro-2-(1-methylethoxy)phenyl]boronic acid

Description:
[3-bromo-5-fluoro-2-(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, making it useful in various applications, particularly in organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a bromine atom and a fluorine atom, which can influence its reactivity and biological activity. The presence of the 1-methylethoxy group enhances its solubility and stability in organic solvents. Boronic acids like this one are often employed in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, the unique combination of halogen substituents may impart specific electronic properties, affecting the compound's reactivity and interaction with biological targets. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry and their potential utility in drug development and materials science.
Formula:C9H11BBrFO3
InChI:InChI=1/C9H11BBrFO3/c1-5(2)15-9-7(10(13)14)3-6(12)4-8(9)11/h3-5,13-14H,1-2H3
SMILES:CC(C)Oc1c(cc(cc1Br)F)B(O)O
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