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Structure of 300-38-9
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3,5-Dibromotyrosine features two bromine atoms at the 3- and 5-positions of the aromatic ring, conferring enhanced electron deficiency and stability. This configuration enables selective incorporation into peptide sequences for radiolabeling studies or bioactive compound synthesis. The molecule exhibits robust bench stability and facilitates site-specific conjugation in synthetic biology workflows.
3,5-Dibromotyrosine serves as a brominated aromatic building block for the synthesis of bioactive peptides and heterocyclic scaffolds. Its dual bromine substituents at the meta positions enhance electrophilic reactivity in Pd-catalyzed cross-coupling reactions, enabling efficient diversification of peptide backbones. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for iterative synthetic workflows in medicinal chemistry and 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-H332-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: