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Structure of 86119-59-7
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4-Bromo-1-methyl-2-phenyl-1H-imidazole integrates a bromine substituent at the C4 position and a methyl group at nitrogen, enabling direct functionalization in cross-coupling reactions. The phenyl ring enhances π-conjugation and solubility in organic media. This bench-stable heterocycle serves as a modular scaffold for synthesizing bioactive imidazoles and transition metal catalysts.
4-Bromo-1-methyl-2-phenyl-1H-imidazole serves as a versatile building block in medicinal chemistry and heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its stable bromine functionality. The methyl and phenyl substituents provide steric and electronic modulation, enhancing reactivity in Suzuki-Miyaura and Buchwald-Hartwig transformations. Its bench-stable nature and ease of purification make it well-suited for iterative synthesis of imidazole-based scaffolds found in pharmaceutical intermediates.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: