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Structure of 1030313-53-1
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This bench-stable hydrazine derivative features a fluorinated aryl group and trifluoromethyl substituent, delivering enhanced electron-withdrawing character. It serves as a key intermediate in the synthesis of heterocyclic compounds, particularly in medicinal chemistry applications where halogenated aromatic systems are required.
(2-Fluoro-4-(trifluoromethyl)phenyl)hydrazine hydrochloride serves as a versatile building block for constructing heterocyclic scaffolds, particularly in the synthesis of pyrazoles and triazoles via cycloaddition reactions. Its stability under standard bench conditions, combined with high functional group tolerance, facilitates efficient incorporation into complex molecular architectures relevant to medicinal chemistry and agrochemical development.
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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: