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Structure of 16711-71-0
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3,5-Diiodo-D-tyrosine features a D-configured tyrosine backbone bearing iodine substituents at the 3 and 5 positions of the aromatic ring. This electron-deficient phenolic scaffold enhances metabolic stability and serves as a key building block for radiolabeled peptides in molecular imaging. The diiodo substitution pattern enables efficient isotopic exchange and facilitates incorporation into bioactive sequences with high fidelity.
3,5-Diiodo-D-tyrosine serves as a valuable building block for the synthesis of iodinated peptide scaffolds and radiolabeled biomolecules. Its D-configured backbone and ortho-diiodo substitution pattern confer enhanced metabolic stability and selective bioorthogonal reactivity, enabling efficient incorporation into therapeutic peptides via solid-phase synthesis. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for applications in radioisotope labeling and targeted drug delivery research.
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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: