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Structure of 66195-39-9
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2-Iodo-6-methoxybenzoic acid features a strategically positioned iodine atom and methoxy group on the aromatic ring, enabling efficient cross-coupling reactions. The carboxylic acid functionality provides a direct handle for peptide coupling or derivatization. This bench-stable reagent combines high reactivity with ease of handling in synthetic workflows.
2-Iodo-6-methoxybenzoic acid serves as a versatile building block for Suzuki-Miyaura and Stille coupling reactions, enabling efficient construction of biaryl and heteroaryl scaffolds. The iodine atom facilitates reliable cross-coupling under standard conditions, while the methoxy and carboxylic acid groups provide orthogonal functional handles for further derivatization. Its bench-stable nature and compatibility with common purification methods make 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 : 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: