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CAS 656239-38-2

:

4-(4-Morpholinylcarbonyl)benzeneboronic acid pinacol ester

Description:
4-(4-Morpholinylcarbonyl)benzeneboronic acid pinacol ester, identified by its CAS number 656239-38-2, is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group and a pinacol ester moiety. This compound features a morpholine ring, which contributes to its solubility and reactivity, making it useful in various organic synthesis applications. The pinacol ester functionality enhances its stability and can facilitate reactions such as Suzuki coupling, a widely used method for forming carbon-carbon bonds. The presence of the morpholinylcarbonyl group suggests potential for biological activity, as morpholine derivatives are often explored in medicinal chemistry. Additionally, the compound's boronic acid characteristics allow for reversible interactions with diols, which can be exploited in sensor applications or drug delivery systems. Overall, this compound is notable for its versatility in synthetic chemistry and potential applications in pharmaceuticals and materials science.
Formula:C17H24BNO4
InChI:InChI=1/C17H24BNO4/c1-16(2)17(3,4)23-18(22-16)14-7-5-13(6-8-14)15(20)19-9-11-21-12-10-19/h5-8H,9-12H2,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2ccc(cc2)C(=O)N2CCOCC2)O1
Synonyms:
  • Methanone, 4-morpholinyl[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-
  • Morpholin-4-yl[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanone
  • 4-{[4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl]Carbonyl}Morpholine
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