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CAS 874289-14-2

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

Description:
[4-(Diethylcarbamoyl)-3-fluoro-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 diethylcarbamoyl group and a fluorine atom, which can influence its reactivity and biological activity. The presence of 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 diethylcarbamoyl group may enhance solubility and stability in various solvents. The fluorine atom can impart unique electronic properties, potentially affecting the compound's interaction with biological targets. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry and their role in developing pharmaceuticals and agrochemicals.
Formula:C11H15BFNO3
InChI:InChI=1/C11H15BFNO3/c1-3-14(4-2)11(15)9-6-5-8(12(16)17)7-10(9)13/h5-7,16-17H,3-4H2,1-2H3
SMILES:CCN(CC)C(=O)c1ccc(cc1F)B(O)O
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