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Structure of 56962-11-9
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2-Chloro-4-hydroxybenzaldehyde features a hydroxyl group flanked by electron-withdrawing chlorine and aldehyde functionalities, enabling direct coupling in heterocyclic synthesis. This ortho-directing system facilitates regioselective functionalization under mild conditions, while the phenolic moiety enhances solubility in polar solvents and supports metal coordination in catalytic systems.
2-Chloro-4-hydroxybenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted benzimidazoles, quinolines, and other heterocyclic scaffolds. The ortho-chloro and para-hydroxyl groups provide complementary sites for electrophilic substitution and coupling reactions, while the aldehyde functionality facilitates reductive amination, Ullmann-type couplings, and condensation reactions. Bench-stable and readily purified by recrystallization, it offers reliable performance 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-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: