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Structure of 1217428-98-2
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Ethyl (E)-2-amino-2-(hydroxyimino)acetate features a stable E-configured oxime moiety that enables selective coupling reactions in peptide synthesis. This bench-stable derivative integrates readily into amide bond formation protocols, offering enhanced reactivity without requiring harsh activation conditions.
Ethyl (E)-2-amino-2-(hydroxyimino)acetate serves as a versatile building block for heterocyclic synthesis, particularly in the construction of oxadiazole and triazole scaffolds. Its stable E-configured hydroxyimino group enables selective coupling reactions under mild conditions, while the amino and ester functionalities offer orthogonal reactivity for downstream functionalization. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for iterative synthetic workflows in medicinal chemistry and process development.
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GHS Pictogram :
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GHS No : GHS02,GHS06
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Signal Word : Danger
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UN#: 2926
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Class : 4.1,6.1
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Packing Group : Ⅲ
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Hazard Statements : H228-H301+H311+H331-H315-H319
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Precautionary Statements : P210-P240-P241-P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P370+P378-P405-P501
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Lot numbers can be found on the outside label of a product: