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Structure of 938-63-6
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4-Amino-2,3,5,6-tetrafluorophenol features a highly electron-deficient aromatic ring stabilized by four fluorine substituents, enabling robust coupling reactions. The amino group provides a reactive handle for conjugation, while the phenolic OH offers directional functionalization. This compound exhibits enhanced metabolic stability and solubility in polar solvents, making it valuable for medicinal chemistry and agrochemical synthesis under standard conditions.
4-Amino-2,3,5,6-tetrafluorophenol serves as a versatile building block in medicinal chemistry, enabling efficient access to fluorinated heterocycles and bioactive scaffolds. Its reactive amino group facilitates nucleophilic substitution and coupling reactions, while the tetrafluoro substitution pattern enhances metabolic stability and modulates electronic properties. The compound exhibits good bench stability and is compatible with standard synthetic protocols, facilitating straightforward purification and integration into complex molecular architectures.
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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: