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Structure of 438450-39-6
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This pyrazole-carboxylic acid features a trifluoromethyl group and a 3-chloropyridin-2-yl moiety, delivering enhanced electron-withdrawing character and improved metabolic stability. The carboxylic acid function enables direct conjugation in synthetic routes, while the chloropyridine unit supports efficient coupling reactions under standard conditions. Designed for use in medicinal chemistry and agrochemical development, this compound integrates readily into complex molecular architectures.
1-(3-Chloropyridin-2-yl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxylic acid serves as a versatile building block for heterocyclic scaffolds in medicinal chemistry, enabling efficient coupling reactions via its carboxylic acid functionality. The trifluoromethyl and chloropyridine groups confer enhanced metabolic stability and favorable electronic properties, while the pyrazole core offers robust bench stability and compatibility with standard synthetic transformations.
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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: