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Structure of 623577-59-3
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4-Bromo-1-(4-fluorophenyl)-1H-imidazole features a bromine-substituted imidazole core paired with a para-fluorophenyl group, delivering enhanced electron-withdrawing character and improved stability under standard reaction conditions. This scaffold integrates readily into cross-coupling processes, enabling efficient access to biologically relevant heterocyclic architectures.
4-Bromo-1-(4-fluorophenyl)-1H-imidazole serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions to construct biaryl and heteroaryl scaffolds. The bromo group facilitates efficient C–C bond formation under standard Suzuki-Miyaura or Stille conditions, while the 4-fluorophenyl substituent enhances metabolic stability and modulates electronic properties. Its bench-stable crystalline form simplifies handling and purification, making it well-suited for iterative synthesis campaigns in API development.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: