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CAS 874289-15-3

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[3-fluoro-4-(propylcarbamoyl)phenyl]boronic acid

Description:
[3-Fluoro-4-(propylcarbamoyl)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 and is widely used in organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a fluorine atom at the meta position and a propylcarbamoyl group at the para position, contributing to its unique chemical reactivity and potential biological activity. The boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, the presence of the fluorine atom can enhance the compound's lipophilicity and influence its pharmacokinetic properties. The propylcarbamoyl group may also impart specific interactions with biological targets, suggesting potential applications in drug development. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry and their significance in the development of pharmaceuticals.
Formula:C10H13BFNO3
InChI:InChI=1/C10H13BFNO3/c1-2-5-13-10(14)8-4-3-7(11(15)16)6-9(8)12/h3-4,6,15-16H,2,5H2,1H3,(H,13,14)
SMILES:CCCN=C(c1ccc(cc1F)B(O)O)O
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