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Structure of 59557-92-5
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2-Bromo-5-methoxyaniline features a bromine substituent at the ortho position relative to the amino group and a methoxy group at the para position, creating a uniquely activated aryl amine. This electronic profile enables direct coupling in Pd-catalyzed cross-coupling reactions without requiring additional protection. The molecule exhibits enhanced solubility in common organic solvents and maintains stability under standard bench conditions, facilitating its use in synthetic workflows targeting functionalized heterocycles and bioactive intermediates.
2-Bromo-5-methoxyaniline serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted anilines via Pd-catalyzed cross-coupling reactions. Its bromine and methoxy functionalities offer orthogonal reactivity for sequential functionalization, while the amine group facilitates direct derivatization or protection. The compound exhibits good bench stability and is compatible with standard purification protocols, making it well-suited for scalable synthesis and high-throughput screening 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: