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Structure of 6952-89-2
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(4-Bromophenyl)(cyclopropyl)methanone features a brominated aromatic ring paired with a cyclopropyl ketone moiety, enabling direct incorporation into cross-coupling and heterocycle-forming reactions. This sterically constrained scaffold delivers enhanced metabolic stability and facilitates efficient derivatization in medicinal chemistry campaigns.
(4-Bromophenyl)(cyclopropyl)methanone serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of biaryl and heterocyclic scaffolds. Its brominated aryl group facilitates palladium-catalyzed cross-coupling reactions, while the cyclopropyl ketone moiety offers stability and compatibility with diverse functional groups. The molecule exhibits excellent bench stability and simplifies 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 : H302
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: