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Structure of 1003709-57-6
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3-Fluoro-4-iodobenzaldehyde features a fluorinated aromatic ring paired with iodine and aldehyde functionalities, enabling direct coupling in cross-coupling reactions. The electron-deficient benzaldehyde moiety facilitates nucleophilic addition, while the ortho-fluoro group enhances regioselectivity in Pd-catalyzed transformations. This bench-stable compound serves as a key intermediate for pharmaceutical and agrochemical synthesis.
3-Fluoro-4-iodobenzaldehyde serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl scaffolds. The ortho-fluoro and para-iodo substituents provide orthogonal reactivity for sequential functionalization, while the aldehyde group offers direct access to imines, oximes, and other downstream derivatives. Bench-stable and compatible with standard reaction conditions, it facilitates streamlined 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-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: