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Structure of 182918-73-6
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Methyl 2-(4-aminophenyl)-2-hydroxyacetate features a phenolic hydroxyl group and a primary amine in para configuration, enabling dual functionalization. This scaffold integrates readily into conjugation workflows and serves as a key intermediate for bioactive compound synthesis under standard conditions.
Methyl 2-(4-aminophenyl)-2-hydroxyacetate serves as a versatile building block for the synthesis of bioactive heterocycles and pharmaceutical intermediates. Its ortho-hydroxyacetate functionality enables facile cyclization reactions, while the para-aminophenyl group offers direct handle for derivatization via coupling or electrophilic substitution. The compound exhibits good bench stability and is compatible with a range of standard synthetic transformations, facilitating efficient access to complex scaffolds 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-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: