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Structure of 2476-29-1
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1-(4-Amino-2-hydroxyphenyl)ethanone features a dual functional group architecture with an electron-rich phenolic hydroxyl and a primary amine positioned ortho to the ketone. This arrangement enables direct integration into bioconjugation workflows and facilitates metal coordination in catalytic systems. The compound exhibits enhanced solubility in polar solvents and stability under standard bench conditions, making it suitable for synthetic intermediates in pharmaceutical and materials chemistry.
1-(4-Amino-2-hydroxyphenyl)ethanone serves as a versatile building block in medicinal chemistry, enabling direct access to hydroxylated and amino-substituted aromatic scaffolds. Its dual functionality—phenolic OH and primary amine—facilitates downstream derivatization via acylation, alkylation, or coupling reactions. The molecule exhibits good bench stability and is compatible with standard purification methods, making it well-suited for iterative synthesis of bioactive compounds and heterocyclic systems.
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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: