(9-Oxo-9H-fluoren-1-yl)boronic acid

98%

Reagent Code: #222281
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CAS Number 194470-10-5

science Other reagents with same CAS 194470-10-5

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inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

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Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the preparation of complex organic molecules, particularly in pharmaceutical and materials chemistry. Its structure allows for the introduction of fluorenone-derived moieties into larger conjugated systems, making it valuable in the development of organic semiconductors, fluorescent dyes, and bioactive compounds. The boronic acid group facilitates palladium-catalyzed coupling with aryl halides, offering versatility in constructing functionalized aromatic frameworks.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,680.00
inventory 250mg
10-20 days ฿4,360.00
inventory 1g
10-20 days ฿12,260.00
inventory 5g
10-20 days ฿50,050.00

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(9-Oxo-9H-fluoren-1-yl)boronic acid
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Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the preparation of complex organic molecules, particularly in pharmaceutical and materials chemistry. Its structure allows for the introduction of fluorenone-derived moieties into larger conjugated systems, making it valuable in the development of organic semiconductors, fluorescent dyes, and bioactive compounds. The boronic acid group facilitates palladium-catalyzed

Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the preparation of complex organic molecules, particularly in pharmaceutical and materials chemistry. Its structure allows for the introduction of fluorenone-derived moieties into larger conjugated systems, making it valuable in the development of organic semiconductors, fluorescent dyes, and bioactive compounds. The boronic acid group facilitates palladium-catalyzed coupling with aryl halides, offering versatility in constructing functionalized aromatic frameworks.

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