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*For research and further manufacturing use only, not for direct human use.
Structure of 50-80-6
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1-(5-Amino-2-hydroxyphenyl)ethanone features a phenolic hydroxyl and primary amine in close proximity, enabling chelation and bifunctional reactivity. This ortho-substituted aryl ketone integrates readily into bioconjugation workflows, offering enhanced solubility and stability under physiological conditions. The scaffold serves as a key intermediate for functionalized aromatic systems in medicinal chemistry and probe development.
1-(5-Amino-2-hydroxyphenyl)ethanone serves as a versatile building block for the synthesis of bioactive heterocycles and pharmaceutical intermediates. The molecule combines an ortho-amino phenol motif with a ketone functionality, enabling straightforward derivatization via condensation, cyclization, or metal-catalyzed coupling reactions. Its bench-stable nature and compatibility with common protecting group strategies facilitate efficient access to complex scaffolds 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: