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Structure of 93415-79-3
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Methyl 2-iodo-3-nitrobenzoate features a strategically positioned iodine and nitro group on a methyl benzoate scaffold, enabling direct functionalization in cross-coupling reactions. The electron-deficient aromatic ring enhances reactivity in palladium-catalyzed transformations, while the ester moiety offers stability and solubility under standard conditions.
Methyl 2-iodo-3-nitrobenzoate serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient C–C bond formation at the iodine site. The ortho-nitro group enhances reactivity and directs regioselective functionalization, while the ester moiety provides stability and ease of purification. This compound facilitates access to substituted aromatic scaffolds relevant in medicinal chemistry and materials science.
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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
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Precautionary Statements : P264-P270-P330
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Lot numbers can be found on the outside label of a product: