For research use only. Not for therapeutic Use.
5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinamide is a boronic ester derivative used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its structure features a nicotinamide ring with a boronate ester group, making it a valuable intermediate for creating complex molecules. This compound is commonly employed in pharmaceutical research for the synthesis of bioactive compounds, including drug candidates. Its stability and reactivity contribute to advancements in medicinal chemistry, allowing for efficient formation of carbon-carbon bonds in drug development.
CAS Number | 1169402-51-0 |
Molecular Formula | C12H17BN2O3 |
Purity | ≥95% |
IUPAC Name | 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-3-carboxamide |
InChI | InChI=1S/C12H17BN2O3/c1-11(2)12(3,4)18-13(17-11)9-5-8(10(14)16)6-15-7-9/h5-7H,1-4H3,(H2,14,16) |
InChIKey | NJLZODHYCOZPBJ-UHFFFAOYSA-N |
Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |