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Structure of 1073354-14-9
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5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)picolinaldehyde features a boronate ester group paired with an aldehyde functionality, enabling direct coupling in Suzuki-Miyaura reactions and selective derivatization. This bench-stable reagent integrates seamlessly into complex molecule synthesis workflows.
5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)picolinaldehyde serves as a versatile boronate building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. The picolinaldehyde moiety provides a synthetically accessible handle for further functionalization, while the stable boronate ester ensures excellent bench stability and compatibility with diverse functional groups. This reagent facilitates the rapid assembly of substituted heteroaromatic scaffolds commonly found in pharmaceutical intermediates 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: