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Structure of 507462-88-6
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This boronate ester features a methoxy-substituted phenol scaffold, enabling direct coupling in Suzuki-Miyaura reactions. The tetramethyl-1,3,2-dioxaborolan-2-yl group provides enhanced stability and compatibility under standard conditions. Designed for efficient cross-coupling workflows, this reagent integrates seamlessly into synthetic sequences requiring precise functional group placement.
3-Methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol serves as a versatile boronate building block in Suzuki-Miyaura cross-coupling reactions. Its ortho-methoxy group enhances solubility and modulates reactivity, while the stable pinacol boronate moiety enables efficient coupling with aryl and vinyl halides under mild conditions. The compound exhibits excellent bench stability, simplifies purification, and is widely used in the construction of biaryl scaffolds for pharmaceutical and materials 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: