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Structure of 72652-32-5
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This trichloroacetophenone derivative features a bromopyrrole moiety that enables direct functionalization in cross-coupling reactions. The electron-deficient ketone group facilitates nucleophilic addition, while the trifluoromethyl-like steric and electronic profile enhances stability under standard conditions.
1-(4-Bromo-1H-pyrrol-2-yl)-2,2,2-trichloroethanone serves as a versatile building block for constructing brominated heterocyclic scaffolds. Its trichloromethyl group enables efficient functionalization via nucleophilic substitution or reduction, while the pyrrole ring provides a platform for further derivatization. The molecule exhibits bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis in medicinal chemistry and process development workflows.
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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-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: