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Structure of 5814-05-1
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(2-Chlorobenzoyl)hydrazine features a chlorinated benzoyl group linked to hydrazine, enabling direct integration into heterocyclic synthesis. This bench-stable reagent facilitates the construction of bioactive pyrazole and triazole frameworks under standard conditions. The ortho-chloro substituent enhances electrophilicity and directs regioselective cyclization.
(2-Chlorobenzoyl)hydrazine serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyrazole and triazole scaffolds via cyclization reactions. Its ortho-chloro substituent enhances electrophilic reactivity while maintaining bench stability and compatibility with common functional groups. The hydrazide moiety facilitates coupling and condensation processes, making it well-suited for medicinal chemistry campaigns requiring modular scaffold construction.
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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 : H315-H319-H335
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Precautionary Statements : P233-P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: