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Structure of 51239-46-4
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This boronate moiety integrates a para-aminomethyl group, enabling direct conjugation to biomolecules via amine-reactive chemistries. The pendant primary amine facilitates site-specific labeling and bioconjugation, while the boronic acid offers stable binding to diols in glycoconjugates. Bench-stable under standard conditions, this reagent streamlines synthesis of targeted probes for chemical biology applications.
(4-(Aminomethyl)phenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl scaffolds under mild conditions. The pendant primary amine facilitates downstream derivatization and orthogonal functional group manipulation, while the boronic acid moiety offers excellent bench stability and compatibility with diverse reaction partners. Its utility is well-established in medicinal chemistry and materials science for constructing complex aromatic architectures with precise structural control.
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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: