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Structure of 74073-40-8
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2-Bromo-3-chlorobenzaldehyde features a dual halogenated aromatic core with strategically positioned bromo and chloro substituents flanking the aldehyde group. This configuration enables selective coupling reactions in cross-coupling protocols and facilitates downstream functionalization in pharmaceutical and agrochemical synthesis. The molecule exhibits enhanced reactivity due to the electron-withdrawing effect of adjacent halogens, while maintaining bench-stable handling characteristics under standard conditions.
2-Bromo-3-chlorobenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The aldehyde group facilitates downstream functionalization via oxidation, reduction, or nucleophilic addition, while the bromo and chloro substituents offer complementary coupling handles for sequential diversification. Bench-stable and compatible with standard purification methods, it functions reliably in multi-step syntheses requiring regioselective transformations.
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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: