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Structure of 105994-77-2
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4-Bromo-1-methyl-5-phenyl-1H-pyrazole features a brominated pyrazole core with a methyl group at N1 and a phenyl substituent at C5, delivering a robust scaffold for medicinal chemistry. The electron-deficient pyrazole ring enables efficient coupling reactions, while the sterically accessible bromine facilitates cross-coupling transformations. This compound exhibits excellent bench stability and solubility in common organic solvents, streamlining its use in synthesis workflows.
4-Bromo-1-methyl-5-phenyl-1H-pyrazole serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its stable bromo functionality. The methyl and phenyl substituents provide orthogonal reactivity handles, while the pyrazole core offers inherent bench stability and compatibility with standard purification methods. This compound facilitates efficient access to substituted pyrazole scaffolds relevant to medicinal chemistry and materials science applications.
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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: