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Structure of 1027513-46-7
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Methyl 3-fluoro-4-iodobenzoate features a fluorinated aryl core paired with a strategically positioned iodine handle, enabling efficient cross-coupling reactions. The electron-withdrawing fluorine enhances reactivity in palladium-catalyzed transformations, while the ester group offers synthetic versatility. This bench-stable reagent integrates seamlessly into complex molecule assembly workflows.
Methyl 3-fluoro-4-iodobenzoate serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient C–C bond formation via palladium-catalyzed Suzuki, Stille, or Negishi processes. The ortho-fluoro and para-iodo substituents provide orthogonal reactivity for sequential functionalization, while the methyl ester group offers stability and ease of purification. Its bench-stable nature and compatibility with standard synthetic workflows make it well-suited for medicinal chemistry and materials 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 : H319
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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: