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Structure of 3107-34-4
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2-(Trifluoromethyl)phenylhydrazine hydrochloride features a trifluoromethyl-substituted phenyl ring paired with a hydrazine functional group, delivering enhanced electrophilic reactivity and improved solubility in polar solvents. This bench-stable derivative facilitates efficient imine and azo compound synthesis under mild conditions.
2-(Trifluoromethyl)phenylhydrazine hydrochloride serves as a versatile building block for heterocyclic synthesis, enabling efficient access to triazoles, pyrazoles, and other nitrogen-containing scaffolds. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in medicinal chemistry campaigns. The hydrochloride salt ensures improved bench stability and ease of handling, while maintaining high reactivity in standard coupling and cyclization protocols.
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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: