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*For research and further manufacturing use only, not for direct human use.
Structure of 1829-22-7
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2-Iodoterephthalic acid features a rigid aromatic core with strategically positioned iodine and carboxylic acid groups, enabling direct functionalization in cross-coupling reactions. This bench-stable derivative supports efficient diversification of polyaromatic scaffolds under standard conditions.
2-Iodoterephthalic acid serves as a versatile building block for palladium-catalyzed cross-coupling reactions, enabling efficient construction of biaryls and extended π-conjugated systems. Its ortho-iodo functionality exhibits high reactivity in Suzuki, Stille, and Negishi couplings, while the carboxylic acid groups provide handles for derivatization or metal coordination. The compound demonstrates excellent bench stability and facilitates straightforward purification, making it well-suited for applications in materials science and medicinal chemistry scaffold synthesis.
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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: