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Structure of 1451390-88-7
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4-Bromo-2-isopropylphenylboronic acid features a boronic acid group flanked by bromine and isopropyl substituents on a phenyl ring, enabling selective cross-coupling in Suzuki-Miyaura reactions. The sterically hindered isopropyl group enhances stability, while the bromine facilitates downstream functionalization. This arylboronic acid delivers predictable reactivity under standard conditions, streamlining access to complex biaryl architectures.
4-Bromo-2-isopropylphenylboronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl scaffolds. Its stability under ambient conditions and compatibility with diverse reaction partners facilitate reliable C–C bond formation. The isopropyl group provides steric bulk that can influence regioselectivity in subsequent transformations, while the bromo substituent offers orthogonal reactivity for sequential functionalization.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: