For research use only. Not for therapeutic Use.
2,3-Dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine(CAT: L031077) is a boronic ester derivative of pyridine, with methyl groups at the 2- and 3-positions on the pyridine ring and a dioxaborolane moiety at the 5-position. The boronic ester group enhances the compound’s reactivity, making it particularly useful in Suzuki-Miyaura coupling reactions, a common method for creating carbon-carbon bonds in organic synthesis. 2,3-Dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is widely utilized in pharmaceutical and material science research as a building block for synthesizing complex aromatic structures, bioactive molecules, and functionalized polymers. Its versatility in coupling reactions makes it essential in drug discovery and the development of agrochemical agents.
Catalog Number | L031077 |
CAS Number | 741709-65-9 |
Molecular Formula | C13H20BNO2 |
Purity | ≥95% |
IUPAC Name | 2,3-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine |
InChI | InChI=1S/C13H20BNO2/c1-9-7-11(8-15-10(9)2)14-16-12(3,4)13(5,6)17-14/h7-8H,1-6H3 |
InChIKey | LBQVSLAREHNEHT-UHFFFAOYSA-N |