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Structure of 1073-69-4
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N-(4-Chlorophenyl)hydrazine features a hydrazine group linked to a para-chlorinated phenyl ring, delivering a potent nucleophilic center for conjugation reactions. This bench-stable compound integrates readily into heterocyclic scaffolds and serves as a key intermediate in the synthesis of azo dyes, pharmaceuticals, and bioactive molecules.
N-(4-Chlorophenyl)hydrazine serves as a reliable building block for the synthesis of hydrazone derivatives and heterocyclic scaffolds, including pyrazoles and triazoles. Its stability under standard bench conditions and compatibility with diverse reaction environments enable efficient coupling and cyclization processes. The para-chloro substituent provides a handle for further functionalization via nucleophilic aromatic substitution, enhancing versatility in medicinal chemistry and materials science applications.
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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-P260-P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: