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 |