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Structure of 589-21-9
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(4-Bromophenyl)hydrazine features a brominated aromatic ring linked to a hydrazine functional group, enabling direct integration into azo dye synthesis and heterocyclic scaffold construction. This bench-stable reagent facilitates efficient coupling reactions under standard conditions, offering reliable access to diverse nitrogen-rich architectures in medicinal chemistry and materials science applications.
(4-Bromophenyl)hydrazine serves as a versatile building block in the synthesis of heterocyclic scaffolds, particularly azo dyes and triazoles. Its hydrazine functionality enables straightforward coupling reactions with carbonyl compounds, aldehydes, and activated esters, facilitating efficient access to biologically relevant architectures. The bromine substituent provides a handle for subsequent cross-coupling transformations, enhancing synthetic 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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: