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Structure of 40276-63-9
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(2-Benzylphenyl)boronic acid features a boronate moiety appended to a benzyl-substituted phenyl ring, enabling efficient Suzuki-Miyaura coupling under standard conditions. The benzylic linker enhances solubility and stability compared to parent arylboronic acids, while the ortho-benzyl group imparts steric control during cross-coupling. This structure facilitates precise C–C bond formation in complex molecule synthesis.
(2-Benzylphenyl)boronic acid serves as a versatile building block in palladium-catalyzed cross-coupling reactions, enabling efficient C–C bond formation under standard Suzuki-Miyaura conditions. Its stability under ambient conditions and compatibility with diverse functional groups facilitate straightforward synthesis of biaryl architectures. The ortho-benzyl substituent enhances regiochemical control in cyclization sequences and provides a handle for further derivatization in medicinal chemistry applications.
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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: