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Structure of 56181-49-8
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2-Bromo-4,6-diphenylpyrimidine features a bromine substituent at the 2-position flanked by two phenyl groups on the pyrimidine core. This electron-deficient heterocycle serves as a key scaffold in medicinal chemistry for constructing kinase inhibitors and functionalized pharmaceutical intermediates. The steric bulk of the diphenyl substitution enhances metabolic stability while enabling selective coupling reactions under standard cross-coupling conditions.
2-Bromo-4,6-diphenylpyrimidine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its well-defined electrophilic bromine site. The diphenyl substitution enhances stability and modulates reactivity, facilitating functionalization at C4 or C6 positions. Its bench-stable solid form simplifies handling and purification, making it ideal for constructing complex pyrimidine-based scaffolds in 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: