CAS 188665-74-9
:3-AMINOCARBONYLPHENYLBORONIC ACID, PINACOL ESTER
Description:
3-Aminocarbonylyphenylboronic acid, pinacol ester, is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group and an amino carbonyl functional group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols and sugars, making it useful in various applications, including organic synthesis and medicinal chemistry. The pinacol ester functionality enhances its stability and solubility, facilitating its use in chemical reactions. The presence of the amino group suggests potential for biological activity, as amines can participate in hydrogen bonding and interact with biological targets. Additionally, the compound may exhibit moderate polarity due to the combination of hydrophobic phenyl and polar functional groups, influencing its solubility in organic solvents. Overall, 3-aminocarbonylyphenylboronic acid, pinacol ester, is a versatile compound with significant implications in synthetic and pharmaceutical chemistry.
Formula:C13H18BNO3
InChI:InChI=1/C13H18BNO3/c1-12(2)13(3,4)18-14(17-12)10-7-5-6-9(8-10)11(15)16/h5-8H,1-4H3,(H2,15,16)
Synonyms:- 3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)-Benzamide
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Found 3 products.
Benzamide, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
CAS:Formula:C13H18BNO3Purity:97%Color and Shape:SolidMolecular weight:247.09793-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-benzamide
CAS:<p>3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-benzamide</p>Purity:98%Molecular weight:247.10g/mol3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-benzamide
CAS:Formula:C13H18BNO3Purity:98%Color and Shape:SolidMolecular weight:247.1


