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Structure of 848093-29-8
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5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinaldehyde features a boronate ester group fused to a pyridine aldehyde scaffold, enabling direct incorporation into Suzuki-Miyaura cross-coupling reactions. The tetramethyl-substituted dioxaborolane moiety imparts enhanced stability and moisture tolerance, while the aldehyde functionality offers a handle for downstream derivatization. This reagent streamlines access to complex heteroaryl aldehydes under standard conditions.
5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinaldehyde serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The aldehyde functionality enables direct functionalization or derivatization, while the stable boronate ester facilitates mild reaction conditions and excellent functional group tolerance. Its bench-stable nature and compatibility with diverse substrates make it ideal for constructing complex heterocyclic scaffolds and pharmaceutical intermediates.
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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: