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Structure of 84388-68-1
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4,5-Dichloro-2-hydroxybenzaldehyde features a benzaldehyde core substituted with two chlorine atoms at the 4 and 5 positions and a hydroxyl group at the 2 position. This electron-deficient aromatic aldehyde integrates readily into coupling reactions, offering enhanced reactivity in synthetic transformations. The ortho-hydroxy arrangement enables chelation effects, stabilizing reaction intermediates. Bench-stable under standard conditions, it serves as a selective building block for complex heterocycles and bioactive molecule synthesis.
4,5-Dichloro-2-hydroxybenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted benzofurans and other heterocyclic scaffolds. The ortho-hydroxyaldehyde functionality facilitates intramolecular cyclization under mild conditions, while the electron-withdrawing dichloro substituents enhance reactivity in electrophilic substitution and coupling reactions. Its bench-stable crystalline form simplifies handling and purification in multi-step syntheses.
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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 : H302-H315-H319-H335
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Precautionary Statements : P261-P302+P352-P304+P340
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Lot numbers can be found on the outside label of a product: