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Structure of 1228183-22-9
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This boronate moiety integrates seamlessly into Suzuki-Miyaura cross-coupling reactions, offering robust stability and compatibility with diverse functional groups. The benzimidazole scaffold enhances solubility and electronic modulation, enabling efficient C–C bond formation under standard conditions.
(1H-Benzo[d]imidazol-6-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl architectures under mild conditions. The boronic acid moiety exhibits excellent bench stability and compatibility with diverse functional groups, facilitating straightforward purification and integration into complex molecular frameworks. Its incorporation into heterocyclic scaffolds supports the synthesis of pharmaceutically relevant compounds and advanced materials.
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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: