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CAS 480438-73-1

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(5-fluoro-2-propoxyphenyl)boronic acid

Description:
(5-Fluoro-2-propoxyphenyl)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 fluorine atom at the 5-position and a propoxy group at the 2-position of a phenyl ring, contributing to its unique electronic and steric properties. These modifications can enhance its reactivity and selectivity in chemical reactions. The boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, the presence of the fluorine atom can influence the compound's lipophilicity and biological activity, making it a candidate for drug development. Overall, (5-fluoro-2-propoxyphenyl)boronic acid exemplifies the versatility of boronic acids in synthetic chemistry and their potential in pharmaceutical applications.
Formula:C9H12BFO3
InChI:InChI=1/C9H12BFO3/c1-2-5-14-9-4-3-7(11)6-8(9)10(12)13/h3-4,6,12-13H,2,5H2,1H3
SMILES:CCCOc1ccc(cc1B(O)O)F
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