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Structure of 1879-58-9
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(3-Cyanophenoxy)acetic acid features a para-cyano-substituted phenoxy scaffold integrated with a carboxylic acid handle, enabling direct conjugation in synthetic and medicinal chemistry workflows. This electron-deficient aryl moiety enhances reactivity in coupling reactions while maintaining stability under standard conditions.
(3-Cyanophenoxy)acetic acid serves as a versatile building block for the synthesis of bioactive heterocycles and pharmaceutical intermediates. Its ortho-cyano and carboxylic acid functionalities enable direct derivatization via amidation, esterification, or cyclization reactions. The molecule exhibits good bench stability and facilitates efficient purification by recrystallization, making it well-suited for scalable medicinal chemistry campaigns and API precursor development.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: