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Structure of 181140-34-1
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This chiral epoxide integrates seamlessly into asymmetric synthesis, where the oxiran-2-ylmethyl moiety enables stereoselective ring-opening reactions. The isoindoline-1,3-dione core provides a rigid, electron-deficient scaffold ideal for conjugate additions and transition-metal-catalyzed transformations under standard conditions.
(R)-2-(oxiran-2-ylmethyl)isoindoline-1,3-dione serves as a versatile chiral building block for the synthesis of complex heterocycles and bioactive molecules. The epoxide moiety enables stereoselective ring-opening reactions with nucleophiles, while the isoindoline-1,3-dione scaffold provides excellent functional group tolerance and stability under standard reaction conditions. Its well-defined stereochemistry facilitates the construction of enantioselective scaffolds relevant to medicinal chemistry and natural product synthesis.
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GHS Pictogram :
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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: