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Structure of 1324054-68-3
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This acetic acid derivative features a chlorinated aromatic ring linked to a methoxycarbonyl group, delivering enhanced solubility and stability under standard conditions. The para-substituted phenyl moiety enables efficient coupling in synthetic transformations, while the carboxylic acid functionality supports direct derivatization in pharmaceutical and agrochemical synthesis workflows.
2-(3-Chloro-4-(methoxycarbonyl)phenyl)acetic acid serves as a versatile building block for pharmaceutical intermediates, enabling efficient construction of biologically relevant heterocyclic scaffolds. Its ortho-chloro and ester functionalities provide orthogonal reactivity for late-stage diversification via palladium-catalyzed cross-coupling or hydrolysis/functionalization sequences. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for scalable synthesis in medicinal chemistry workflows.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: