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CAS 933986-97-1

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6-(1-Pyrrolidinyl)pyridine-3-boronic acid pinacol ester

Description:
6-(1-Pyrrolidinyl)pyridine-3-boronic acid pinacol ester, identified by its CAS number 933986-97-1, is a chemical compound that features a pyridine ring substituted with a pyrrolidine group and a boronic acid moiety. This compound is characterized by its boronic ester functionality, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the pyrrolidine group may enhance its solubility and reactivity, while the boronic acid component is significant in Suzuki coupling reactions, a key method for forming carbon-carbon bonds. The pinacol ester form provides stability and can facilitate the handling and storage of the boronic acid. Overall, this compound is of interest in the development of pharmaceuticals and agrochemicals, owing to its potential reactivity and functional versatility in synthetic pathways.
Formula:C15H23BN2O2
InChI:InChI=1/C15H23BN2O2/c1-14(2)15(3,4)20-16(19-14)12-7-8-13(17-11-12)18-9-5-6-10-18/h7-8,11H,5-6,9-10H2,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2ccc(nc2)N2CCCC2)O1
Synonyms:
  • 2-Pyrrolidin-1-Yl-5-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Pyridine
  • 6-(Pyrrolidin-1-Yl)Pyridine-3-Boronic Acid, Pinacol Ester
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