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Structure of 41327-15-5
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5-Bromo-3-methyl-1-phenyl-1H-pyrazole features a brominated pyrazole core with a methyl group at the 3-position and a phenyl substituent at N1, delivering enhanced electronic modulation and steric profile. This bench-stable heterocycle integrates readily into cross-coupling workflows and serves as a key scaffold in medicinal chemistry for targeted kinase inhibition and bioactive molecule construction.
5-Bromo-3-methyl-1-phenyl-1H-pyrazole serves as a versatile building block in medicinal chemistry and heterocyclic synthesis. The bromo group enables palladium-catalyzed cross-coupling reactions, while the methyl and phenyl substituents provide defined steric and electronic profiles. Its stability under standard reaction conditions facilitates purification and integration into complex molecular architectures.
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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-P405-P501
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Lot numbers can be found on the outside label of a product: