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Structure of 27143-07-3
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Ethyl chloro[(4-methoxyphenyl)hydrazono]acetate features a hydrazone linkage flanked by a methoxy-substituted phenyl ring and a chloroacetyl group, delivering enhanced reactivity in heterocyclic synthesis. This bench-stable, moisture-tolerant reagent integrates seamlessly into multistep transformations, enabling efficient access to functionalized pyrazole derivatives under standard conditions.
Ethyl chloro[(4-methoxyphenyl)hydrazono]acetate serves as a versatile hydrazone-based building block for the synthesis of heterocyclic scaffolds, particularly in the construction of pyrazole and triazole derivatives. Its stability under standard laboratory conditions and compatibility with diverse functional groups facilitate efficient transformations in medicinal chemistry workflows. The compound enables regioselective cyclizations and functions effectively in both solution-phase and solid-phase synthesis applications.
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GHS No : GHS06,GHS08
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331-H341
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P405-P501
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Lot numbers can be found on the outside label of a product: