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CAS 1309981-33-6

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B-[6-(2-Methyl-1-piperidinyl)-2-pyridinyl]boronic acid

Description:
B-[6-(2-Methyl-1-piperidinyl)-2-pyridinyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols and other nucleophiles. This compound features a pyridine ring substituted with a piperidine moiety, contributing to its potential biological activity and interaction with various biological targets. The presence of the boronic acid group suggests applications in medicinal chemistry, particularly in drug design and development, as boronic acids are often utilized in the synthesis of pharmaceuticals and as tools in biochemical research. The compound's structure may also impart specific solubility and reactivity characteristics, making it suitable for various chemical reactions, including Suzuki coupling reactions, which are pivotal in forming carbon-carbon bonds. Overall, B-[6-(2-Methyl-1-piperidinyl)-2-pyridinyl]boronic acid exemplifies the versatility of boronic acids in both synthetic and medicinal chemistry contexts.
Formula:C11H17BN2O2
InChI:InChI=1S/C11H17BN2O2/c1-9-5-2-3-8-14(9)11-7-4-6-10(13-11)12(15)16/h4,6-7,9,15-16H,2-3,5,8H2,1H3
InChI key:InChIKey=GYFDCVGRCYXICV-UHFFFAOYSA-N
SMILES:CC1N(C=2N=C(B(O)O)C=CC2)CCCC1
Synonyms:
  • B-[6-(2-Methyl-1-piperidinyl)-2-pyridinyl]boronic acid
  • Boronic acid, B-[6-(2-methyl-1-piperidinyl)-2-pyridinyl]-
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