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Structure of 1028263-94-6
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4-Fluoro-3-iodoanisole features a strategically positioned iodine atom adjacent to a methoxy group, enabling efficient cross-coupling reactions. The fluorine substituent enhances metabolic stability and modulates electronic properties. This ortho-haloaryl scaffold serves as a key building block in pharmaceutical synthesis, particularly for constructing biologically active heterocycles under palladium catalysis.
4-Fluoro-3-iodoanisole serves as a versatile building block in cross-coupling chemistry, enabling efficient construction of biaryl and heterocyclic scaffolds. The ortho-iodo group facilitates reliable palladium-catalyzed coupling reactions, while the para-fluoro substituent offers enhanced metabolic stability and strategic positioning for further functionalization. Its bench-stable nature and compatibility with standard reaction conditions make it ideal for iterative synthesis in medicinal chemistry and materials science applications.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: