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Structure of 255724-71-1
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5-Fluoro-2-iodoaniline features a fluorine atom at the 5-position and an iodine substituent at the 2-position of the aniline ring, creating a highly functionalized aryl scaffold. This electron-deficient platform enables efficient cross-coupling reactions, particularly in palladium-catalyzed transformations. The molecule exhibits excellent stability under standard conditions and serves as a key intermediate for synthesizing bioactive compounds and advanced materials.
5-Fluoro-2-iodoaniline serves as a versatile building block for Suzuki-Miyaura and Ullmann-type coupling reactions, enabling efficient construction of biaryl scaffolds. Its ortho-iodo functionality exhibits high reactivity under standard palladium catalysis, while the meta-fluoro group offers orthogonal handle for further functionalization. The compound demonstrates 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 : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H412
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Precautionary Statements : P264-P270-P273-P330-P405-P501
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Lot numbers can be found on the outside label of a product: