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Structure of 524740-42-9
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5-Bromo-1-methyl-3-(trifluoromethyl)-1H-pyrazole features a trifluoromethyl group that enhances electron deficiency and metabolic stability, while the bromine substituent enables facile functionalization via cross-coupling. This pyrazole scaffold integrates readily into bioactive molecules, offering improved solubility and compatibility in medicinal chemistry applications.
5-Bromo-1-methyl-3-(trifluoromethyl)-1H-pyrazole serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its stable bromo and electron-deficient trifluoromethyl groups. The molecule exhibits excellent bench stability, facilitates straightforward purification, and functions effectively in Suzuki-Miyaura and Buchwald-Hartwig transformations for constructing complex heterocyclic scaffolds.
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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: