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Structure of 3107-33-3
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(3-(Trifluoromethyl)phenyl)hydrazine hydrochloride features a trifluoromethyl-substituted phenyl ring paired with a hydrazine functional group, delivering enhanced electron-withdrawing character and improved stability under standard bench conditions. This moisture-tolerant reagent integrates readily into heterocyclic synthesis and facilitates efficient coupling reactions in medicinal chemistry workflows.
(3-(Trifluoromethyl)phenyl)hydrazine hydrochloride serves as a versatile building block for heterocyclic synthesis, particularly in the construction of triazoles, indoles, and other nitrogen-containing scaffolds. Its trifluoromethyl group imparts enhanced metabolic stability and lipophilicity, making it valuable in medicinal chemistry applications. The hydrochloride salt ensures excellent bench stability and ease of handling, while the hydrazine functionality enables reliable coupling reactions under standard conditions.
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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: