CAS 943911-66-8
:N-(2-hydroxyethyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
Description:
N-(2-hydroxyethyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide is a chemical compound characterized by its unique structure, which includes a benzamide moiety and a boron-containing dioxaborolane group. This compound features a hydroxyethyl substituent that enhances its solubility in polar solvents, making it suitable for various applications in organic synthesis and medicinal chemistry. The presence of the dioxaborolane group suggests potential utility in boron chemistry, particularly in reactions involving boron as a Lewis acid or in the formation of organoboron compounds. The tetramethyl substitution on the dioxaborolane ring contributes to its stability and steric hindrance, which can influence reactivity and selectivity in chemical reactions. Additionally, the compound may exhibit interesting biological properties due to the amide functional group, which can participate in hydrogen bonding and molecular interactions. Overall, this compound represents a versatile building block in the development of new materials and pharmaceuticals, with potential applications in drug discovery and chemical research.
Formula:C15H22BNO4
InChI:InChI=1/C15H22BNO4/c1-14(2)15(3,4)21-16(20-14)12-7-5-6-11(10-12)13(19)17-8-9-18/h5-7,10,18H,8-9H2,1-4H3,(H,17,19)
SMILES:CC1(C)C(C)(C)OB(c2cccc(c2)C(=NCCO)O)O1
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Found 3 products.
N-[2-Hydroxyethyl]benzamide-3-boronic acid, pinacol ester
CAS:Formula:C15H22BNO4Purity:96%Color and Shape:SolidMolecular weight:291.1505N-[2-Hydroxyethyl]benzamide-3-boronic acid, pinacol ester
CAS:<p>N-[2-Hydroxyethyl]benzamide-3-boronic acid, pinacol ester</p>Purity:96%Molecular weight:291.15g/molN-(2-Hydroxyethyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
CAS:Purity:96%Molecular weight:291.1499939


