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Structure of 14572-89-5
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1-(4-Aminophenyl)ethan-1-ol features a phenolic hydroxyl group flanked by an electron-rich aromatic ring and a primary amine, enabling versatile conjugation in bioconjugate chemistry. This bench-stable scaffold integrates readily into peptide and small-molecule constructs under standard conditions, offering enhanced solubility and reactivity for targeted labeling applications.
1-(4-Aminophenyl)ethan-1-ol serves as a versatile building block for pharmaceutical and agrochemical synthesis, enabling direct access to arylated amine scaffolds. Its dual functionality—phenolic hydroxyl and primary amine—facilitates sequential derivatization, including acylation, etherification, and coupling reactions. The compound exhibits good bench stability and is readily purified by recrystallization or chromatography, supporting scalable applications in medicinal chemistry campaigns.
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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: