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Structure of 5455-98-1
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This oxirane-functional isoindoline derivative integrates a reactive epoxide ring with a rigid, electron-deficient isoindoline scaffold. The strained oxirane moiety enables selective nucleophilic ring opening under mild conditions, facilitating conjugation to amines or thiols in bioconjugation workflows. Designed for stability during storage and ease of handling, this compound serves as a robust linker in the synthesis of targeted therapeutics and functionalized polymers.
2-(Oxiran-2-ylmethyl)isoindoline-1,3-dione serves as a versatile bifunctional building block, enabling efficient construction of complex heterocyclic scaffolds. The epoxide moiety facilitates regioselective ring-opening reactions with nucleophiles, while the phthalimide group offers excellent stability and compatibility with standard synthetic protocols. Its bench-stable nature and predictable reactivity make it ideal for modular synthesis in medicinal chemistry and process development workflows.
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H318
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
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Lot numbers can be found on the outside label of a product: