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Structure of 1252793-57-9
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This boronate ester features a rigid indenyl scaffold that enhances stability and reactivity in cross-coupling processes. The tetramethyl-substituted dioxaborolane ring ensures excellent shelf life and moisture tolerance, enabling reliable use under standard conditions. Its defined stereochemistry and electron-rich character facilitate efficient coupling with aryl halides and pseudohalides.
2-(2,3-Dihydro-1H-inden-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boron building block for Suzuki-Miyaura cross-coupling reactions. The indenyl moiety provides a rigid, electron-rich aryl framework with predictable reactivity, enabling efficient C–C bond formation under standard catalytic conditions. Its tetramethyl-substituted dioxaborolane enhances shelf stability and facilitates purification, making it well-suited for iterative synthesis and library generation 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: