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Structure of 57631-11-5
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5-Bromo-3-(trifluoromethyl)-1H-indazole features a unique combination of bromine and trifluoromethyl substituents on the indazole scaffold, delivering enhanced electron-withdrawing character and improved metabolic stability. This configuration enables efficient coupling in transition-metal-catalyzed transformations, making it a valuable building block for medicinal chemistry and functional materials synthesis.
5-Bromo-3-(trifluoromethyl)-1H-indazole serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its well-defined bromine and trifluoromethyl functionalities. Its stability under standard reaction conditions and compatibility with diverse coupling partners facilitate efficient construction of complex heterocyclic scaffolds. The molecule's defined electronic profile enhances regioselective transformations, making it a practical choice for API intermediate synthesis and drug discovery campaigns.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H315-H319-H335
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: