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Structure of 20637-09-6
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Methyl 4-(4-aminophenyl)butanoate features a para-aminophenyl group linked via a butanoate chain, enabling integration into conjugation workflows. The electron-rich aromatic ring and amine functionality support facile derivatization, while the ester moiety offers tunable reactivity under standard conditions. This compound serves as a key intermediate in bioconjugation and pharmaceutical synthesis.
Methyl 4-(4-aminophenyl)butanoate serves as a versatile building block for the synthesis of aromatic amides and heterocyclic scaffolds. Its pendant aniline functionality enables direct coupling reactions, while the ester group facilitates selective transformations under standard conditions. The molecule exhibits good bench stability and is readily purified by crystallization or column chromatography, making it well-suited for iterative medicinal chemistry campaigns and process-scale applications.
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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: