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CAS 938043-31-3

:

1-Piperidinyl[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanone

Description:
1-Piperidinyl[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanone, with the CAS number 938043-31-3, is a synthetic organic compound characterized by its complex structure that includes a piperidine ring and a boron-containing dioxaborolane moiety. This compound typically exhibits properties such as moderate solubility in organic solvents and potential reactivity due to the presence of the boron atom, which can participate in various chemical reactions, including Suzuki coupling. The piperidine ring contributes to its basicity and potential biological activity, making it of interest in medicinal chemistry. The presence of the dioxaborolane group may enhance its stability and reactivity in certain conditions, making it useful in organic synthesis and material science. Overall, this compound's unique structural features suggest potential applications in pharmaceuticals and agrochemicals, although specific biological activity and reactivity would depend on further empirical studies.
Formula:C18H26BNO3
InChI:InChI=1S/C18H26BNO3/c1-17(2)18(3,4)23-19(22-17)15-10-8-14(9-11-15)16(21)20-12-6-5-7-13-20/h8-11H,5-7,12-13H2,1-4H3
InChI key:InChIKey=YOXMAOLZXRIELZ-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC=C(C(=O)N3CCCCC3)C=C2
Synonyms:
  • 1-Piperidinyl[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanone
  • [4-(Piperidine-1-carbonyl)phenyl]boronic acid pinacol ester
  • Methanone, 1-piperidinyl[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-
  • 4-(PIPERIDINE-1-CARBONYL)PHENYLBORONIC ACID PINACOL ESTER
  • 4-(1-PIPERIDINYLCARBONYL)BENZENEBORONIC ACID PINACOL ESTER
  • 4-(PIPERIDINE)CARBOXAMIDOPHENYLBORONIC ACID, PINACOL ESTER
  • 1-[4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)BENZOYL]PIPERIDINE
  • Piperidin-1-yl(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanone
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