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Structure of 476004-81-6
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This boronate-functionalized indole integrates seamlessly into Suzuki-Miyaura cross-coupling reactions under standard conditions. The tetramethyl-1,3,2-dioxaborolane moiety provides enhanced stability and moisture tolerance, enabling reliable use in synthetic workflows. The indole core offers a privileged scaffold for medicinal chemistry and materials applications.
2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole serves as a versatile boronate building block in palladium-catalyzed cross-coupling reactions. Its stability under ambient conditions and tolerance to diverse functional groups enable reliable C–C bond formation with aryl and vinyl halides. The indole core provides a privileged scaffold for medicinal chemistry applications, while the boronate moiety facilitates efficient synthesis of biologically relevant heterocyclic architectures.
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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: