2,6-Dichloro-4-hydroxy-3,5-dimethoxybenzaldehyde
95%
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Used as an intermediate in the synthesis of complex organic compounds, particularly in pharmaceutical research for developing antimicrobial, antioxidant, and antihypertensive drugs. It features a reactive aldehyde group along with chlorine substituents at positions 2 and 6, and methoxy and hydroxy groups at 3, 4, and 5 on the benzene ring, enabling the construction of specialized benzaldehyde derivatives that enhance binding affinity to biological targets. Commonly employed in research for bioactive compounds, natural product analogs, and fluorescent probes for laboratory assays, where its structure can generate luminescent signals upon reaction with specific substances. Its functional groups support selective chemical modifications, making it valuable in medicinal chemistry and drug discovery.
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