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Structure of 52411-34-4
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This bifunctional aniline derivative features a rigid, electron-rich aromatic core with strategically positioned ether linkages and amine groups. The ortho-aminophenoxy substitution pattern enables efficient coordination in metal complexation and facilitates conjugation in polymer architectures. Designed for synthetic versatility, it integrates seamlessly into advanced materials and bioactive molecule scaffolds under standard conditions.
2-[2-(2-Aminophenoxy)ethoxy]aniline serves as a versatile bifunctional building block for constructing complex heterocyclic scaffolds and bioactive molecules. Its dual aniline and ether functionalities enable robust coupling reactions, including Ullmann-type aryl-aryl couplings and metal-catalyzed cross-couplings. The molecule exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis in medicinal chemistry and materials science applications.
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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: