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Structure of 52159-67-8
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Methyl 3-chloro-2-hydroxybenzoate features a chlorinated aromatic ring with ortho-hydroxyl and ester functionalities, enabling direct incorporation into bioactive scaffolds. The hydroxyl group facilitates hydrogen bonding in molecular recognition, while the methyl ester provides a handle for selective derivatization under mild conditions. This compound exhibits enhanced solubility in organic solvents compared to its parent acid, streamlining purification and reaction monitoring.
Methyl 3-chloro-2-hydroxybenzoate serves as a versatile building block in medicinal chemistry and synthetic organic workflows. The ortho-hydroxyl group enables direct functionalization or coordination in transition metal catalysis, while the methyl ester provides a handle for selective hydrolysis or coupling reactions. The chlorine substituent offers moderate electrophilic reactivity, facilitating nucleophilic substitution under controlled conditions. Its bench-stable nature and compatibility with standard purification methods make it well-suited for multi-step synthesis of heterocyclic scaffolds and bioactive molecules.
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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: