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Structure of 177167-53-2
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2,6-Dichloro-4-iodobenzaldehyde features a sterically hindered aromatic core with complementary halogen substituents enabling selective cross-coupling. The aldehyde group provides a reactive handle for nucleophilic addition and condensation reactions. This compound serves as a key intermediate in the synthesis of functionalized heterocycles and bioactive molecules under standard conditions.
2,6-Dichloro-4-iodobenzaldehyde serves as a versatile building block for the synthesis of functionalized aromatic scaffolds, leveraging its orthogonal halogenation pattern for sequential cross-coupling reactions. The aldehyde group enables direct derivatization via imine formation or reductive amination, while the iodine facilitates palladium-catalyzed coupling under mild conditions. Bench-stable and compatible with standard purification methods, it supports efficient access to complex heterocycles and drug-like intermediates in medicinal chemistry 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: