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Structure of 85107-55-7
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4-Methoxycarbonyl-2-nitrophenylboronic acid features a boronic acid handle flanked by electron-withdrawing nitro and ester groups, enhancing reactivity in Suzuki-Miyaura couplings. The para-nitro substitution stabilizes the boronate intermediate, while the methoxycarbonyl moiety provides a handle for downstream functionalization. This bench-stable reagent streamlines access to complex aromatic scaffolds under standard conditions.
4-Methoxycarbonyl-2-nitrophenylboronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl architectures. The ortho-nitro and ester functionalities provide orthogonal reactivity for downstream transformations, while the boronic acid group offers excellent bench stability and compatibility with diverse reaction conditions. Its defined substitution pattern facilitates predictable regiochemistry in complex molecule assembly.
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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: