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Structure of 874831-02-4
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Ethyl 3-chloro-4-iodobenzoate features a strategically positioned chloro and iodo substituent on the benzoate scaffold, enabling selective cross-coupling reactions. The electron-deficient aromatic ring facilitates palladium-catalyzed transformations, while the ethyl ester group offers a handle for downstream derivatization. This compound serves as a key intermediate in the synthesis of functionalized biaryl systems and pharmaceutical candidates requiring halogen-directed coupling.
Ethyl 3-chloro-4-iodobenzoate serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl scaffolds. The ortho-chloro and para-iodo substituents provide complementary reactivity for sequential functionalization, with the chloro group undergoing palladium-catalyzed substitution under robust conditions. Its bench-stable nature and compatibility with standard purification protocols make it ideal for iterative synthesis in medicinal chemistry and process development workflows.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: