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Structure of 1026989-94-5
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2,3-Difluoro-4-iodoaniline features a fluorinated aromatic core with complementary electron-withdrawing substituents, enabling precise tuning of reactivity in cross-coupling and electrophilic substitution. The iodine handle facilitates efficient palladium-catalyzed transformations, while the difluoro groups enhance metabolic stability and modulate electronic properties for applications in medicinal chemistry and materials synthesis.
2,3-Difluoro-4-iodoaniline serves as a versatile building block for the synthesis of fluorinated heterocycles and pharmaceutical intermediates. Its ortho-difluoro substitution enhances metabolic stability, while the iodine handle enables palladium-catalyzed cross-coupling reactions. The compound exhibits good bench stability and facilitates efficient functionalization in standard coupling protocols, making it well-suited for medicinal chemistry applications requiring precise fluorination and late-stage diversification.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: