CAS 874289-47-1
:[5-(diethylcarbamoyl)-2-fluoro-phenyl]boronic acid
Description:
[5-(Diethylcarbamoyl)-2-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. This compound features a phenyl ring substituted with a fluorine atom and a diethylcarbamoyl group, which enhances its solubility and reactivity. The presence of the boronic acid moiety allows for participation in cross-coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, the diethylcarbamoyl group may contribute to the compound's stability and influence its biological activity. The fluorine substitution can also affect the electronic properties of the molecule, potentially enhancing its reactivity or selectivity in chemical reactions. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry and their applications in drug development and material science.
Formula:C11H15BFNO3
InChI:InChI=1/C11H15BFNO3/c1-3-14(4-2)11(15)8-5-6-10(13)9(7-8)12(16)17/h5-7,16-17H,3-4H2,1-2H3
SMILES:CCN(CC)C(=O)c1ccc(c(c1)B(O)O)F
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Found 3 products.
N,N-Diethyl 3-borono-4-fluorobenzamide
CAS:Formula:C11H15BFNO3Purity:97%Color and Shape:SolidMolecular weight:239.05115-(Diethylcarbamoyl)-2-fluorobenzeneboronic acid
CAS:<p>5-(Diethylcarbamoyl)-2-fluorobenzeneboronic acid</p>Purity:97%Molecular weight:239.05g/mol(5-(Diethylcarbamoyl)-2-fluorophenyl)boronic acid
CAS:Formula:C11H15BFNO3Purity:97%Color and Shape:SolidMolecular weight:239.05


