For research use only. Not for therapeutic Use.
(3-Chloropyridin-2-yl)boronic acid(Cat No.:L006723), is a chemical compound essential in organic synthesis, particularly in medicinal and materials chemistry. As a boronic acid derivative, it is pivotal in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its unique structure, incorporating a chloropyridine moiety, enhances its reactivity and specificity, making it valuable for modifying biologically active compounds or designing novel materials. Researchers employ (3-Chloropyridin-2-yl)boronic acid as a versatile building block, significantly contributing to advancements in drug discovery, materials science, and the creation of specialized chemicals for various industrial applications.
| CAS Number | 1448866-17-8 |
| Molecular Formula | C5H5BClNO2 |
| Purity | ≥95% |
| IUPAC Name | (3-chloropyridin-2-yl)boronic acid |
| InChI | InChI=1S/C5H5BClNO2/c7-4-2-1-3-8-5(4)6(9)10/h1-3,9-10H |
| InChIKey | QBKWMNFYLXBEDV-UHFFFAOYSA-N |
| SMILES | B(C1=C(C=CC=N1)Cl)(O)O |
| Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |