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Structure of 1453472-98-4
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This trifluoropropylhydrazine hydrochloride delivers a highly electron-deficient hydrazine moiety, enabling selective coupling in nucleophilic substitution reactions. Its bench-stable, moisture-tolerant form simplifies handling during synthetic workflows.
(1,1,1-Trifluoropropan-2-yl)hydrazine hydrochloride serves as a stable, bench-ready building block for the synthesis of trifluoromethylated hydrazine derivatives. Its trifluoromethyl group imparts enhanced metabolic stability and lipophilicity, making it valuable in medicinal chemistry applications. The compound readily participates in condensation reactions with carbonyl compounds to form hydrazone scaffolds, enabling access to diverse heterocyclic systems. Functional group tolerance and ease of purification support its utility in multi-step syntheses.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: