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Structure of 2613-34-5
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3-Chloro-2,4-difluoroaniline features a strategically positioned chloro and two fluoro substituents that enhance electron withdrawal and metabolic stability. This bench-stable aryl amine integrates readily into pharmaceutical intermediates and agrochemical scaffolds, offering predictable reactivity in coupling and cyclization processes under standard conditions.
3-Chloro-2,4-difluoroaniline serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of heterocyclic scaffolds via electrophilic substitution and coupling reactions. Its ortho-fluoro substituents facilitate directed metallation and Suzuki-Miyaura coupling, while the chloro group provides a handle for nucleophilic displacement. The compound exhibits good bench stability and is compatible with standard purification protocols, making it well-suited for iterative synthetic campaigns requiring functional group tolerance and predictable reactivity.
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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: