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Structure of 145123-24-6
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2-Amino-3-bromobenzaldehyde features a strategically positioned bromine atom and an amino group flanking the aldehyde functionality, enabling direct incorporation into transition-metal-catalyzed cross-coupling reactions. This electron-rich scaffold supports rapid diversification in pharmaceutical intermediates and functional materials synthesis under standard conditions.
2-Amino-3-bromobenzaldehyde serves as a versatile building block in medicinal chemistry and heterocyclic synthesis, enabling efficient access to substituted quinoline and benzimidazole scaffolds. Its ortho-functionalized structure facilitates regioselective coupling reactions and transition-metal-catalyzed transformations. The aldehyde group offers direct utility for reductive amination, Schiff base formation, and Ugi-type multicomponent reactions, while the amino and bromo substituents provide orthogonal handles for further derivatization. Bench-stable and compatible with standard purification protocols, it supports scalable synthesis workflows.
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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: