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Structure of 52787-19-6
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This acetic acid derivative features a methoxycarbonyl-substituted phenyl ring, enabling direct incorporation into peptide conjugation and bioconjugate workflows. The ortho-carboxylic acid group provides enhanced reactivity for amide bond formation under standard coupling conditions, while the ester moiety offers tunable hydrolytic stability in biological environments.
2-(3-(Methoxycarbonyl)phenyl)acetic acid serves as a versatile building block for constructing biaryl and heterocyclic scaffolds in medicinal chemistry. Its carboxylic acid and ester functionalities enable direct derivatization via amidation, esterification, or decarboxylation protocols. The molecule exhibits good bench stability and facilitates efficient purification by crystallization or column chromatography, making it well-suited for scalable synthesis 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-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: