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Structure of 51839-16-8
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5-Iodoisophthalic acid features a rigid aromatic core with two carboxylic acid groups flanking a para-iodo substituent, enabling precise functionalization in cross-coupling reactions. This configuration supports efficient derivatization for bioconjugation and materials synthesis under standard conditions.
5-Iodoisophthalic acid serves as a versatile building block for metal-catalyzed cross-coupling reactions, enabling efficient access to functionalized aromatic scaffolds. Its iodine substituent facilitates palladium-catalyzed coupling with boronic acids, stannanes, and amines, while the two carboxylic acid groups provide sites for derivatization, salt formation, or incorporation into polymers and bioactive molecules. Bench-stable and readily purified by recrystallization, it functions effectively in standard synthetic workflows requiring ortho-functionalized isophthalate motifs.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: