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Structure of 4114-28-7
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Diethyl hydrazine-1,2-dicarboxylate serves as a key scaffold for synthesizing heterocyclic compounds via cyclization reactions. The molecule features two ester groups flanking a hydrazine moiety, enabling selective coupling and ring formation under mild conditions. This bench-stable reagent facilitates efficient access to pyrazole and triazole derivatives in medicinal chemistry applications.
Diethyl hydrazine-1,2-dicarboxylate serves as a versatile synthon in heterocyclic synthesis, enabling efficient access to pyrazole and triazole scaffolds via cyclization with electrophiles or under thermal conditions. Its dual ester functionality offers compatibility with standard coupling protocols, while the hydrazine moiety provides high reactivity in cycloaddition and condensation reactions. Bench-stable and readily purified by chromatography, it functions as a practical building block for medicinal chemistry campaigns requiring nitrogen-rich heterocycles.
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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#: 2930
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Class : 6.1,4.1
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Packing Group : Ⅱ
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Hazard Statements : H228-H301
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Precautionary Statements : P210-P240-P241-P264-P270-P280-P330-P370+P378-P405-P501
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Lot numbers can be found on the outside label of a product: