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Structure of 2923-56-0
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4-Trifluoromethylphenyl hydrazine hydrochloride delivers a robust, bench-stable platform for constructing heterocyclic scaffolds. The para-trifluoromethyl group enhances electron deficiency and metabolic stability, while the hydrazine moiety enables efficient coupling reactions under mild conditions. This reagent integrates seamlessly into synthetic workflows requiring high functional group tolerance and predictable reactivity.
4-Trifluoromethylphenyl hydrazine hydrochloride serves as a reliable building block for heterocyclic synthesis, enabling efficient access to pyrazoles and triazoles via cycloaddition reactions. Its bench-stable form facilitates handling and purification, while the electron-withdrawing trifluoromethyl group enhances electrophilic reactivity in coupling processes. Functions effectively in standard azo-coupling and cyclization workflows common in medicinal chemistry and materials science.
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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: