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Structure of 851452-58-9
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This acrylamide derivative features a prop-2-en-1-yloxy-substituted phenyl group and a 1,3-dioxindan moiety, combining electron-rich aromaticity with a reactive α,β-unsaturated carbonyl system. The molecule integrates seamlessly into bioconjugation workflows, offering enhanced stability under standard conditions while enabling site-specific labeling via Michael addition.
N-(1,3-Dioxaindan-5-yl)-2-chloro-N-{[2-(prop-2-en-1-yloxy)phenyl]methyl}acetamide serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of complex heterocyclic scaffolds. Its pendant allyl ether and chloroacetamide functionalities provide orthogonal reactivity for sequential transformations. The dioxindole core offers enhanced stability and facilitates downstream derivatization, while the overall structure supports mild reaction conditions and straightforward purification—ideal for medicinal chemistry campaigns and process development workflows.
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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#: 1760
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H318-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: