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Structure of 339-59-3
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4-(Trifluoromethyl)benzohydrazide features a trifluoromethyl group that imparts enhanced electron-withdrawing character and metabolic stability, enabling efficient coupling in hydrazone-based conjugation strategies. The hydrazide moiety delivers reliable reactivity under mild conditions, facilitating site-specific labeling in bioconjugation workflows.
4-(Trifluoromethyl)benzohydrazide serves as a versatile building block for the synthesis of heterocyclic scaffolds, particularly in the construction of pyrazole and triazole derivatives via condensation reactions. Its trifluoromethyl group imparts enhanced metabolic stability and lipophilicity, making it valuable in medicinal chemistry campaigns. The hydrazide functionality enables reliable coupling with aldehydes and ketones under mild conditions, offering excellent bench stability and straightforward purification.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: