2,2',7,7'-Tetrakis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9,9'-spirobi[fluorene]

95%

Reagent Code: #130190
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CAS Number 934391-22-7

science Other reagents with same CAS 934391-22-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 820.24 g/mol
Formula C₄₉H₆₀B₄O₈
inventory_2 Storage & Handling
Density 1.18±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions for the preparation of conjugated polymers and small-molecule semiconductors. Its spirobifluorene core provides structural rigidity and thermal stability, making it valuable in the development of materials for organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and perovskite solar cells. The boronate ester groups allow for efficient and selective coupling with aryl halides, enabling the construction of complex π-conjugated systems with tunable electronic properties. Commonly employed in hole-transport materials and as a building block in high-performance optoelectronic devices.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,050.00
inventory 250mg
10-20 days ฿8,590.00
inventory 1g
10-20 days ฿22,000.00

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2,2',7,7'-Tetrakis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9,9'-spirobi[fluorene]
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Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions for the preparation of conjugated polymers and small-molecule semiconductors. Its spirobifluorene core provides structural rigidity and thermal stability, making it valuable in the development of materials for organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and perovskite solar cells. The boronate ester groups allow for efficient and selective coupling with aryl halides, enabling

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions for the preparation of conjugated polymers and small-molecule semiconductors. Its spirobifluorene core provides structural rigidity and thermal stability, making it valuable in the development of materials for organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and perovskite solar cells. The boronate ester groups allow for efficient and selective coupling with aryl halides, enabling the construction of complex π-conjugated systems with tunable electronic properties. Commonly employed in hole-transport materials and as a building block in high-performance optoelectronic devices.

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