For research use only. Not for therapeutic Use.
2-Chlorophenylboronic acid (Cat No.: R025456) is an organoboron compound featuring a boronic acid functional group attached to a chlorinated phenyl ring at the ortho position. It is widely used in Suzuki–Miyaura cross-coupling reactions for forming carbon–carbon bonds, making it a valuable building block in organic synthesis, pharmaceuticals, and materials science. The ortho-chloro substitution adds electronic and steric effects that can influence reaction selectivity. This compound is essential for constructing biaryl structures, agrochemicals, and active pharmaceutical ingredients with precise functional group arrangements.
CAS Number | 3900-89-8 |
Synonyms | (o-Chlorophenyl)boronic Acid; 2-Chlorobenzeneboronic Acid; 2-Chlorophenylboronic Acid; (2-Chlorophenyl)-boronic Acid; o-Chloro-benzeneboronic Acid |
Molecular Formula | C6H6BClO2 |
Purity | ≥95% |
Storage | -20°C |
IUPAC Name | (2-chlorophenyl)boronic acid |
InChI | InChI=1S/C6H6BClO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4,9-10H |
InChIKey | RRCMGJCFMJBHQC-UHFFFAOYSA-N |
SMILES | B(C1=CC=CC=C1Cl)(O)O |
Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |