For research use only. Not for therapeutic Use.
2,6-Dichloro-4-hydroxybenzaldehyde(Cat No.:L029192)is an aromatic compound characterized by two chlorine atoms at the 2 and 6 positions, a hydroxyl group at the 4-position, and an aldehyde functional group at the 1-position on the benzene ring. This unique substitution pattern imparts both electron-withdrawing and electron-donating effects, influencing its reactivity in electrophilic and nucleophilic aromatic substitution reactions. It serves as a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and dyes. The compound’s phenolic and aldehyde functionalities also enable Schiff base formation and other derivatizations important for developing bioactive molecules.
| CAS Number | 60964-09-2 |
| Molecular Formula | C7H4Cl2O2 |
| Purity | ≥95% |
| IUPAC Name | 2,6-dichloro-4-hydroxybenzaldehyde |
| InChI | InChI=1S/C7H4Cl2O2/c8-6-1-4(11)2-7(9)5(6)3-10/h1-3,11H |
| InChIKey | WWFRBIPLCLSKNH-UHFFFAOYSA-N |
| SMILES | C1=C(C=C(C(=C1Cl)C=O)Cl)O |
| Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |