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CAS 874289-58-4

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[2-fluoro-5-(methoxycarbamoyl)phenyl]boronic acid

Description:
[2-Fluoro-5-(methoxycarbamoyl)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, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a fluorine atom and a methoxycarbamoyl group, which contributes to its chemical reactivity and solubility properties. The presence of the boronic acid moiety allows for participation in cross-coupling reactions, such as Suzuki-Miyaura coupling, facilitating the formation of carbon-carbon bonds. Additionally, the methoxycarbamoyl group may enhance the compound's biological activity and solubility in organic solvents. Overall, this compound is of interest in the development of pharmaceuticals and agrochemicals, where its unique structural features can be leveraged for specific chemical transformations and biological interactions.
Formula:C8H9BFNO4
InChI:InChI=1/C8H9BFNO4/c1-15-11-8(12)5-2-3-7(10)6(4-5)9(13)14/h2-4,13-14H,1H3,(H,11,12)
SMILES:CON=C(c1ccc(c(c1)B(O)O)F)O
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