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Structure of 92022-07-6
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4-Bromo-3-methyl-1,1'-biphenyl features a sterically hindered biphenyl core with complementary halogen and alkyl substituents. This configuration enables selective cross-coupling reactions under palladium catalysis, delivering functionalized biaryl architectures with high regiocontrol. The molecule exhibits robust stability under standard bench conditions and integrates efficiently into synthetic sequences requiring precise substitution patterns.
4-Bromo-3-methyl-1,1'-biphenyl serves as a versatile building block in cross-coupling reactions, enabling efficient construction of biaryl scaffolds under palladium-catalyzed conditions. The bromo group facilitates reliable Suzuki, Stille, and Negishi couplings, while the methyl substituent provides steric and electronic modulation. Bench-stable and readily purified by column chromatography, it functions effectively in medicinal chemistry campaigns and materials synthesis.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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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-H318-H413
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Precautionary Statements : P264-P270-P273-P280-P305+P351+P338-P330-P501
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Lot numbers can be found on the outside label of a product: