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*For research and further manufacturing use only, not for direct human use.
Structure of 3743-22-4
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2-Dimethylaminophenol delivers a highly electron-rich phenolic scaffold with enhanced solubility and stability under standard conditions. The dimethylamino group imparts strong resonance donation, increasing nucleophilicity at the ortho position. This enables efficient coupling in oxidative transformations and facilitates incorporation into redox-active molecular architectures.
2-Dimethylaminophenol serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized heterocycles and electron-rich aromatic systems. Its phenolic hydroxyl group facilitates straightforward derivatization, while the ortho-dimethylamino substituent enhances electron donation and supports metal-catalyzed coupling reactions. The compound exhibits good bench stability and is readily purified by recrystallization or column chromatography, making it well-suited for use in medicinal chemistry and materials science applications.
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GHS Pictogram :
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GHS No : GHS05,GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅱ
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Hazard Statements : H301-H315-H318-H335-H412
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: