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Structure of 387845-49-0
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tert-Butyl (1-(bromomethyl)cyclopropyl)carbamate delivers a cyclopropyl ring tethered to a bromomethyl group, enabling direct functionalization at the strained ring junction. The tert-butyl carbamate moiety provides stability and ease of removal under mild acidic conditions. This reagent facilitates efficient incorporation of cyclopropyl motifs into complex molecular architectures.
tert-Butyl (1-(bromomethyl)cyclopropyl)carbamate serves as a versatile building block for cyclopropyl-containing scaffolds in medicinal chemistry. The bromomethyl group enables efficient nucleophilic substitution, facilitating C–C and C–heteroatom bond formation under mild conditions. Its tert-butyl carbamate protection offers excellent bench stability and compatibility with diverse reaction environments, simplifying purification and enabling sequential functionalization. This reagent is particularly valuable for constructing bioactive cyclopropyl motifs 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 : 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: