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Structure of 524955-09-7
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3-Chloro-4-(pyridin-2-ylmethoxy)aniline features a pyridin-2-ylmethoxy group that enhances solubility and modulates electronic properties, while the chloro substituent provides a reactive handle for further functionalization. This scaffold integrates seamlessly into pharmaceutical intermediates and advanced materials due to its stability and compatibility with diverse synthetic transformations.
3-Chloro-4-(pyridin-2-ylmethoxy)aniline serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocycles through standard coupling and functional group manipulation. Its pyridinylmethyl ether moiety provides orthogonal reactivity and enhanced solubility, while the chloro and aniline functionalities facilitate further derivatization via palladium-catalyzed cross-coupling and electrophilic substitution. The compound exhibits good bench stability and is amenable to purification by chromatography or recrystallization, making it well-suited for iterative synthesis in API development.
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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: