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Structure of 22717-55-1
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Methyl 4-chloro-2-hydroxybenzoate features a strategically positioned chloro group at the para position relative to the hydroxyl, enhancing electrophilic reactivity while maintaining stability under standard conditions. The ester functionality enables direct incorporation into synthetic sequences without derivatization. This compound serves as a key intermediate in the synthesis of bioactive heterocycles and functionalized aromatics, particularly in medicinal chemistry applications requiring halogenated phenolic motifs.
Methyl 4-chloro-2-hydroxybenzoate serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted benzene scaffolds. The ortho-hydroxyl group facilitates direct coupling reactions or metal-catalyzed transformations, while the methyl ester offers a handle for selective reduction or hydrolysis. Its bench-stable nature and compatibility with diverse functional groups make it well-suited for multi-step syntheses requiring robust reactivity and predictable transformation pathways.
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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: