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Structure of 656-66-6
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3-Fluoro-4-iodoaniline features a strategically positioned fluorine atom and iodine substituent on the aromatic ring, enabling direct incorporation into cross-coupling reactions. This electron-deficient aniline derivative offers enhanced reactivity in palladium-catalyzed transformations while maintaining bench-stable handling characteristics.
3-Fluoro-4-iodoaniline serves as a versatile building block for palladium-catalyzed cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl scaffolds. The ortho-fluoro and para-iodo substituents provide orthogonal reactivity, facilitating sequential functionalization. Bench-stable and compatible with standard purification methods, it supports scalable synthesis of pharmaceutical intermediates and advanced materials.
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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 : H302-H312-H331
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: