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CAS 480438-60-6

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(4-fluoro-2-propoxyphenyl)boronic acid

Description:
(4-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 phenyl ring substituted with a fluorine atom at the para position and a propoxy group at the ortho position relative to the boronic acid group. This substitution pattern can influence its reactivity and solubility. Typically, boronic acids are polar and can exhibit good solubility in organic solvents, which is beneficial for their use in cross-coupling reactions, such as Suzuki coupling. Additionally, the presence of the fluorine atom may enhance the compound's electronic properties, potentially affecting its biological activity. Overall, (4-fluoro-2-propoxyphenyl)boronic acid is a versatile compound with applications in pharmaceuticals and materials science, particularly in the development of boron-containing drugs and catalysts.
Formula:C9H12BFO3
InChI:InChI=1/C9H12BFO3/c1-2-5-14-9-6-7(11)3-4-8(9)10(12)13/h3-4,6,12-13H,2,5H2,1H3
SMILES:CCCOc1cc(ccc1B(O)O)F
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