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Structure of 651030-56-7
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This boronate-functionalized ethanol derivative integrates a stable tetramethylboronate group with a pendant hydroxyl, enabling efficient Suzuki-Miyaura cross-coupling under standard conditions. The para-substituted aryl scaffold facilitates selective reaction pathways in synthetic sequences.
2-(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethanol serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. Its stable tetramethylboronate group enables efficient C–C bond formation under mild conditions, while the pendant ethylene glycol handle provides solubility and facilitates purification. The molecule exhibits excellent bench stability and functional group tolerance, making it ideal for constructing complex aryl-containing scaffolds in medicinal chemistry and materials science applications.
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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: