For research use only. Not for therapeutic Use.
(6-((Benzyloxy)carbonyl)pyridin-3-yl)boronic acid（Cat No.:L031538）is a functionalized heteroaromatic compound combining a pyridine ring substituted with a boronic acid at the 3-position and a benzyloxycarbonyl (Cbz) protecting group at the 6-position. This molecule is especially valuable in cross-coupling reactions, such as Suzuki-Miyaura coupling, for constructing C–C bonds in pharmaceutical and material chemistry. The boronic acid moiety enables versatile derivatization, while the Cbz group protects amines or alcohols during multistep synthesis. Its structural features support selective reactivity and synthetic flexibility in designing biologically active compounds and complex aromatic systems.
| CAS Number | 1000269-51-1 |
| Molecular Formula | C13H12BNO4 |
| Purity | ≥95% |
| IUPAC Name | (6-phenylmethoxycarbonylpyridin-3-yl)boronic acid |
| InChI | InChI=1S/C13H12BNO4/c16-13(19-9-10-4-2-1-3-5-10)12-7-6-11(8-15-12)14(17)18/h1-8,17-18H,9H2 |
| InChIKey | ZJFHFVUWFKEFTI-UHFFFAOYSA-N |
| SMILES | B(C1=CN=C(C=C1)C(=O)OCC2=CC=CC=C2)(O)O |
| Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |
