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Structure of 1402393-56-9
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This sterically encumbered biphenyl features three isopropyl groups and two methoxy substituents that enhance solubility and stability under standard conditions. The bromine atom enables efficient cross-coupling reactions, while the electron-donating methoxy groups facilitate selective functionalization in catalytic transformations.
2-Bromo-2',4',6'-triisopropyl-3,6-dimethoxy-1,1'-biphenyl serves as a sterically hindered, electron-rich aryl bromide enabling efficient Suzuki-Miyaura coupling under mild conditions. The triisopropyl and dimethoxy substituents enhance solubility and stability while minimizing undesired side reactions. Functions effectively as a building block for complex biaryl 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: