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Structure of 59430-62-5
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This bench-stable arylalanine derivative features a para-aminophenyl moiety linked to a propanoic acid side chain, enabling direct incorporation into peptide conjugates and bioconjugation workflows. The electron-rich aromatic ring facilitates efficient coupling reactions under standard conditions, while the primary amine supports further functionalization.
2-(4-Aminophenyl)propanoic acid serves as a versatile building block for pharmaceutical and agrochemical synthesis, enabling efficient access to biologically relevant arylalanine scaffolds. Its ortho-substituted aniline functionality facilitates direct coupling reactions and downstream derivatization, while the carboxylic acid group supports amide formation and esterification under standard conditions. The compound exhibits good bench stability and is compatible with common purification methods, making it suitable for both small-scale medicinal chemistry campaigns and process development 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: