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CAS 1218790-49-8

:

N-2-Propyn-1-yl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide

Description:
N-2-Propyn-1-yl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide is a chemical compound characterized by its unique structural features, which include a propynyl group and a dioxaborolane moiety. The presence of the dioxaborolane ring contributes to its potential reactivity, particularly in cross-coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The compound is likely to exhibit moderate to high lipophilicity due to the aromatic benzamide structure, which can influence its solubility and bioavailability. Additionally, the presence of the boron atom in the dioxaborolane can facilitate various chemical transformations, including Suzuki coupling reactions. The compound's functional groups suggest potential applications in drug development and materials science. As with many boron-containing compounds, it may also exhibit unique properties such as fluorescence or specific reactivity patterns in the presence of nucleophiles. Overall, this compound represents a versatile building block in synthetic organic chemistry, with implications for both academic research and industrial applications.
Formula:C16H20BNO3
InChI:InChI=1S/C16H20BNO3/c1-6-11-18-14(19)12-7-9-13(10-8-12)17-20-15(2,3)16(4,5)21-17/h1,7-10H,11H2,2-5H3,(H,18,19)
InChI key:InChIKey=BUZIZNWTLHGQQO-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC=C(C(NCC#C)=O)C=C2
Synonyms:
  • N-2-Propyn-1-yl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
  • Benzamide, N-2-propyn-1-yl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
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