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Structure of 1313738-80-5
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1-Benzyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine features a boronate ester group paired with a benzyl-substituted tetrahydropyridine core, enabling efficient Suzuki-Miyaura coupling. This bench-stable reagent integrates readily into complex molecule synthesis, offering reliable C–C bond formation under mild conditions.
1-Benzyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine serves as a versatile boronate building block for palladium-catalyzed cross-coupling reactions. The tetrahydropyridine core provides a stable, bench-ready scaffold with good functional group tolerance, enabling efficient access to substituted heterocyclic architectures. Its pendant benzyl group enhances solubility and stability, while the pinacol boronate moiety facilitates reliable coupling under mild conditions, making it ideal for iterative synthesis in medicinal chemistry and API development.
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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-H413
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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: