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Structure of 238088-31-8
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This boronate ester integrates a nitrile group at the 3-position, enabling direct functionalization via cross-coupling. The tetramethyl-1,3,2-dioxaborolane moiety provides enhanced stability and reactivity under standard conditions. Designed for efficient synthesis of aryl nitriles, this reagent facilitates C–C bond formation with minimal decomposition.
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)propanenitrile serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The nitrile group provides orthogonal functionality for downstream transformations, while the sterically protected boronate ester ensures excellent bench stability and compatibility with diverse reaction conditions. Its predictable reactivity and ease of purification make it ideal for constructing complex molecular architectures in medicinal chemistry and materials science.
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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-H312-H315-H319-H332-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: