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Structure of 383126-84-9
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4-(3,4-Difluorophenoxy)aniline features a fluoro-substituted aromatic ether linkage paired with an aniline handle, delivering enhanced electron density and metabolic stability. This scaffold integrates readily into bioactive molecule design, particularly in kinase inhibitors and CNS-targeted pharmaceuticals. The para-aniline group enables efficient coupling reactions under standard conditions.
4-(3,4-Difluorophenoxy)aniline serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocycles and pharmaceutical scaffolds. Its dual functionality—phenolic ether and primary aromatic amine—facilitates diverse coupling reactions and derivatization strategies. The molecule exhibits good bench stability and compatibility with standard purification methods, making it well-suited for iterative synthesis workflows in API development.
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GHS No : GHS05,GHS07,GHS09
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Signal Word : Danger
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H302-H317-H318-H410
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Precautionary Statements : P261-P264-P270-P272-P273-P280-P302+P352-P330-P362+P364-P391-P501
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Lot numbers can be found on the outside label of a product: