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Structure of 1073353-89-5
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This boronate reagent features a 2-fluoro-4-nitrophenyl group coupled to a stable dioxaborolane core, enabling efficient Suzuki-Miyaura coupling. The electron-deficient aryl moiety enhances reactivity, while the tetramethyl substitution ensures excellent shelf stability and moisture tolerance under standard conditions.
2-(2-Fluoro-4-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. Its ortho-fluoro and para-nitro substituents enable selective functionalization and facilitate downstream transformations in heterocyclic and pharmaceutical scaffold construction. The tetramethyl-substituted dioxaborolane core offers enhanced stability, ease of purification, and compatibility with diverse reaction conditions.
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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: