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*For research and further manufacturing use only, not for direct human use.
Structure of 196207-58-6
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This boronate ester features a fluorene core functionalized with a sterically shielded diborane moiety, enabling efficient Suzuki-Miyaura coupling under standard conditions. The bulky dioctyl substituents enhance solubility and stability, while the tetramethyl-1,3,2-dioxaborolane ring ensures high reactivity and moisture tolerance in synthetic workflows.
2-[9,9-Dioctyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)fluoren-2-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a robust boron-containing building block for Suzuki-Miyaura cross-coupling reactions. Its fluorene core provides structural rigidity and electronic stability, while the sterically protected boronate ester enables high functional group tolerance and bench-stable handling. This compound facilitates efficient construction of complex conjugated systems and extended π-frameworks in materials and pharmaceutical synthesis.
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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: