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Structure of 957062-56-5
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4-Bromo-1-(4-fluorophenyl)-1H-pyrazole features a bromine atom at the C4 position and a para-fluorophenyl group attached to the pyrazole ring, delivering enhanced electron-withdrawing character. This scaffold enables efficient coupling in cross-coupling reactions, particularly under palladium catalysis, and serves as a key building block in medicinal chemistry for targeted drug discovery.
4-Bromo-1-(4-fluorophenyl)-1H-pyrazole serves as a versatile building block for constructing bioactive heterocycles, enabling palladium-catalyzed cross-coupling reactions with broad functional group tolerance. The bromo substituent facilitates Suzuki, Stille, and Negishi couplings, while the 4-fluorophenyl group enhances metabolic stability and modulates electronic properties. This compound exhibits excellent bench stability and simplifies purification, making it ideal for iterative synthesis in medicinal chemistry and process development workflows.
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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-H312-H315-H319-H332-H335
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Precautionary Statements : P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: