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Structure of 1072-52-2
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2-(1-Aziridinyl)ethanol features a strained three-membered aziridine ring linked to an ethanolic side chain, enabling efficient nucleophilic ring-opening reactions. This bifunctional scaffold integrates readily into bioconjugation workflows and synthetic intermediates requiring reactive heterocyclic moieties under mild conditions.
2-(1-Aziridinyl)ethanol serves as a versatile building block in synthetic organic chemistry, enabling efficient access to nitrogen-containing heterocycles and bioactive scaffolds. Its reactive aziridine ring facilitates regioselective ring-opening reactions with nucleophiles, while the pendant hydroxyl group offers a handle for derivatization or protection. The compound exhibits good bench stability and is compatible with standard functional group transformations, making it a practical reagent for medicinal chemistry and process development workflows.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: