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CAS 1171897-39-4

:

tert-butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-ylcarbamate

Description:
Tert-butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-ylcarbamate is a chemical compound characterized by its complex structure, which includes a pyridine ring, a carbamate functional group, and a boron-containing moiety. The presence of the tert-butyl group contributes to its hydrophobic properties, while the dioxaborolane ring enhances its reactivity, particularly in organic synthesis and potential applications in medicinal chemistry. This compound is likely to exhibit moderate to high stability under standard conditions, but its reactivity can be influenced by the presence of functional groups and the overall electronic environment. It may participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it valuable in the development of pharmaceuticals and agrochemicals. Additionally, the compound's solubility and stability in different solvents can vary, which is important for its practical applications in laboratory settings. As with many boron-containing compounds, it may also exhibit unique properties related to coordination chemistry and catalysis.
Formula:C16H25BN2O4
InChI:InChI=1S/C16H25BN2O4/c1-14(2,3)21-13(20)19-12-8-11(9-18-10-12)17-22-15(4,5)16(6,7)23-17/h8-10H,1-7H3,(H,19,20)
SMILES:CC(C)(C)OC(=Nc1cc(cnc1)B1OC(C)(C)C(C)(C)O1)O
Synonyms:
  • tert-butyl N-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridyl]carbamate
  • Carbamic acid, N-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]-, 1,1-dimethylethyl ester
  • [5-(4,4,5,5-Tetramethyl-[1,3,2]Dioxaborolan-2-Yl)Pyridin-3-Yl]Carbamic Acid Tert-Butyl Ester
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