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Structure of 239074-27-2
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tert-Butyl (4-(bromomethyl)phenyl)carbamate features a bromomethyl group appended to a para-substituted phenyl ring, enabling direct functionalization in cross-coupling and nucleophilic substitution reactions. The tert-butyl carbamate moiety provides robust protection for primary amines, offering stability under standard conditions while allowing straightforward deprotection when required. This bifunctional architecture supports efficient synthesis of complex arylamines and conjugated systems.
tert-Butyl (4-(bromomethyl)phenyl)carbamate serves as a versatile building block in synthetic organic chemistry, enabling efficient introduction of a bromomethyl group adjacent to an aromatic ring. The carbamate protection stabilizes the amine during multistep synthesis, while the pendant bromide facilitates palladium-catalyzed couplings and nucleophilic substitutions. Its bench-stable nature and compatibility with standard reaction conditions make it ideal for constructing biaryl scaffolds and functionalized heterocycles in medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314-H318
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P363-P405-P501
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Lot numbers can be found on the outside label of a product: