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Structure of 861932-08-3
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3-Bromo-4-(1H-imidazol-1-yl)benzaldehyde features a brominated aromatic ring paired with a strategically positioned imidazole moiety, enabling direct incorporation into transition metal-catalyzed cross-coupling reactions. The aldehyde group provides a reactive handle for downstream derivatization, while the electron-rich imidazole enhances solubility and facilitates coordination in catalytic systems. This scaffold offers high functional group tolerance and stability under standard bench conditions.
3-Bromo-4-(1H-imidazol-1-yl)benzaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient construction of heterocyclic scaffolds via Suzuki-Miyaura and Buchwald-Hartwig couplings. The aldehyde functionality facilitates direct derivatization, while the bromo and imidazole groups offer orthogonal reactivity for sequential functionalization. Bench-stable and compatible with standard purification methods, it supports scalable synthesis of bioactive molecules.
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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: