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CAS 380499-66-1

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(4-{5-[4-(dimethylamino)phenyl]-1,3-oxazol-2-yl}phenyl)boronic acid

Description:
(4-{5-[4-(Dimethylamino)phenyl]-1,3-oxazol-2-yl}phenyl)boronic acid, with CAS number 380499-66-1, is a boronic acid derivative characterized by its unique structural features. It contains 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 presence of a dimethylamino group enhances its solubility and can influence its electronic properties, potentially affecting its reactivity and interaction with biological targets. The oxazole ring contributes to the compound's stability and may also play a role in its biological activity. This compound is typically used in research settings, particularly in the development of pharmaceuticals and as a building block in organic synthesis. Its properties, such as solubility, stability, and reactivity, can vary depending on the solvent and conditions used in experiments. Overall, this compound exemplifies the versatility of boronic acids in chemical research and applications.
Formula:C17H17BN2O3
InChI:InChI=1/C17H17BN2O3/c1-20(2)15-9-5-12(6-10-15)16-11-19-17(23-16)13-3-7-14(8-4-13)18(21)22/h3-11,21-22H,1-2H3
SMILES:CN(C)c1ccc(cc1)c1cnc(c2ccc(cc2)B(O)O)o1
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