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Structure of 1197050-28-4
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3-Bromo-2-chlorobenzaldehyde features a sterically constrained aromatic core with complementary halogen substituents, enabling selective cross-coupling reactions. The aldehyde group provides a reactive handle for nucleophilic additions and condensation chemistry under standard conditions. This molecule integrates seamlessly into complex synthetic sequences requiring precise functional group placement.
3-Bromo-2-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 functionality facilitates downstream transformations such as reductive amination and Wittig olefination, while the bromo and chloro substituents offer complementary sites for selective functionalization. Bench-stable and readily purified by distillation, it functions effectively in multi-step syntheses requiring precise regiocontrol.
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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: