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Structure of 109240-30-4
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1-(4-Bromophenyl)cyclopropanol features a cyclopropanol ring fused to a brominated aromatic phenyl group, delivering a rigid, electron-deficient scaffold ideal for transition metal-catalyzed coupling reactions. The pendant hydroxyl group enables direct functionalization or derivatization under standard conditions. This bench-stable compound serves as a key building block in medicinal chemistry and materials synthesis.
1-(4-Bromophenyl)cyclopropanol serves as a versatile building block for medicinal chemistry and materials science, enabling direct functionalization at the aryl bromide site via palladium-catalyzed cross-coupling. The cyclopropanol moiety provides a rigid, sterically constrained scaffold with predictable stereochemical behavior. Its bench-stable solid form facilitates handling and purification, while tolerance to diverse reaction conditions supports downstream transformations including oxidation, derivatization, and heterocycle formation in multi-step syntheses.
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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: