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Structure of 276866-90-1
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4-Chloro-3-iodobenzaldehyde features a dual-heteroatom substitution pattern on the aromatic ring, delivering enhanced reactivity in cross-coupling processes. The aldehyde group enables direct functionalization, while the iodine moiety serves as a high-efficiency handle for palladium-catalyzed transformations. This compound exhibits excellent stability under standard bench conditions and integrates readily into complex molecular architectures.
4-Chloro-3-iodobenzaldehyde serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling the construction of biaryl scaffolds under palladium-mediated conditions. The ortho-iodo and para-chloro substituents provide orthogonal reactivity for sequential functionalization, while the aldehyde group offers direct access to imines, hydrazones, and other downstream transformations. Bench-stable and compatible with standard purification methods, it facilitates efficient synthesis of complex aromatic intermediates for medicinal chemistry and materials 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: