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CAS 852227-96-4

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1-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]piperidine

Description:
1-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]piperidine, with the CAS number 852227-96-4, is an organic compound characterized by its unique structural features. It contains a piperidine ring, which is a six-membered nitrogen-containing heterocycle, and a phenyl group substituted with a boron-containing moiety, specifically a tetramethyl-1,3,2-dioxaborolane. This dioxaborolane structure is notable for its ability to form stable complexes with various substrates, making it useful in organic synthesis and medicinal chemistry. The presence of the boron atom enhances the compound's reactivity and potential applications in cross-coupling reactions, particularly in the formation of carbon-carbon bonds. Additionally, the tetramethyl groups contribute to the compound's steric bulk, influencing its solubility and interaction with other molecules. Overall, this compound exemplifies the intersection of boron chemistry and organic synthesis, with potential implications in drug development and materials science.
Formula:C17H26BNO2
InChI:InChI=1S/C17H26BNO2/c1-16(2)17(3,4)21-18(20-16)14-8-10-15(11-9-14)19-12-6-5-7-13-19/h8-11H,5-7,12-13H2,1-4H3
InChI key:InChIKey=OTOKWHGMHAAFRM-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC=C(C=C2)N3CCCCC3
Synonyms:
  • 1-[4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl]Piperidine
  • 2-(4-Piperidinophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • Piperidine, 1-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-
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