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Structure of 75676-72-1
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2-Chloro-4-iodoanisole features a strategically positioned chloro and iodo substituent on an aromatic ring, enabling selective cross-coupling reactions. The methoxy group enhances solubility and directs regiochemistry in palladium-catalyzed transformations. This bench-stable compound serves as a key intermediate in the synthesis of functionalized aryl building blocks for pharmaceutical and materials applications.
2-Chloro-4-iodoanisole serves as a versatile building block in cross-coupling reactions, enabling efficient construction of biaryl scaffolds under Pd-catalyzed conditions. The ortho-chloro and para-iodo substituents provide complementary reactivity for sequential functionalization, while the methoxy group offers moderate electronic stabilization and enhanced solubility. Bench-stable and readily purified by column chromatography, it facilitates reliable synthesis of complex heterocycles and pharmaceutical intermediates.
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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: