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Structure of 5457-29-4
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This isoindoline-1,3-dione derivative features a 3-iodopropyl side chain enabling facile conjugation via palladium-catalyzed coupling. The electron-deficient dione core enhances reactivity in nucleophilic addition processes, while the iodide serves as a robust handle for further functionalization. Bench-stable and moisture-tolerant, it streamlines synthesis of bioconjugates and advanced intermediates.
2-(3-Iodopropyl)isoindoline-1,3-dione serves as a versatile bifunctional building block for medicinal chemistry and materials synthesis. The iodide group enables palladium-catalyzed cross-coupling reactions, while the phthalimide moiety provides a stable, easily removable nitrogen protecting group. Its bench-stable nature and compatibility with diverse reaction conditions facilitate efficient functionalization in multistep syntheses.
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GHS Pictogram :
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GHS No : GHS06,GHS08
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331-H341
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P405-P501
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Lot numbers can be found on the outside label of a product: