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Structure of 266306-18-7
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N-Boc-4-bromo-L-phenylalanine methyl ester features a brominated aromatic ring and a protected amine, enabling direct incorporation into peptide chains under standard coupling conditions. The Boc group ensures stability during synthesis, while the methyl ester facilitates efficient derivatization. This building block supports the construction of complex bioactive peptides with halogenated aromatic functionality.
N-Boc-4-bromo-L-phenylalanine methyl ester serves as a versatile building block in peptide synthesis and medicinal chemistry, enabling site-selective functionalization via palladium-catalyzed cross-coupling. The Boc group provides orthogonal protection for the amine, while the bromo and ester functionalities offer complementary handles for downstream transformations. Bench-stable and readily purified by flash chromatography, it facilitates efficient access to complex scaffolds 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: