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Structure of 2314-36-5
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3,5-Dichloro-4-hydroxybenzaldehyde features a hydroxyl group ortho to the aldehyde, enabling direct participation in hydrogen bonding and condensation reactions. The electron-withdrawing dichloro substituents enhance electrophilicity at the carbonyl carbon, facilitating nucleophilic addition. This bench-stable compound serves as a key building block for bioactive heterocycles and functionalized aromatics in medicinal chemistry and materials synthesis.
3,5-Dichloro-4-hydroxybenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted benzaldehyde scaffolds. Its ortho-hydroxyl and dichloro substituents provide enhanced reactivity for electrophilic substitution, Suzuki coupling, and direct functionalization. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthetic campaigns requiring regioselective derivatization.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: