9,9-Bis(2-ethylhexyl)-2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)fluorene

98%

Reagent Code: #147571
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CAS Number 357219-41-1

science Other reagents with same CAS 357219-41-1

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Weight 642.58 g/mol
Formula C₄₁H₆₄B₂O₄
badge Registry Numbers
MDL Number MFCD16621099
inventory_2 Storage & Handling
Storage Room temperature

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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of conjugated polymers and organic semiconductors. Its boronate ester groups enable efficient carbon-carbon bond formation, making it valuable in the development of organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and field-effect transistors (OFETs). The 2-ethylhexyl side chains enhance solubility in organic solvents, facilitating solution-processing techniques essential for large-area electronic devices. Commonly employed in polymerization reactions to introduce fluorene units into donor-acceptor copolymers, contributing to tunable bandgaps and improved charge transport properties.

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inventory 200mg
10-20 days ฿2,288.00

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9,9-Bis(2-ethylhexyl)-2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)fluorene
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of conjugated polymers and organic semiconductors. Its boronate ester groups enable efficient carbon-carbon bond formation, making it valuable in the development of organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and field-effect transistors (OFETs). The 2-ethylhexyl side chains enhance solubility in organic solvents, facilitating solution-processing techniques essential for large-area electronic

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of conjugated polymers and organic semiconductors. Its boronate ester groups enable efficient carbon-carbon bond formation, making it valuable in the development of organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and field-effect transistors (OFETs). The 2-ethylhexyl side chains enhance solubility in organic solvents, facilitating solution-processing techniques essential for large-area electronic devices. Commonly employed in polymerization reactions to introduce fluorene units into donor-acceptor copolymers, contributing to tunable bandgaps and improved charge transport properties.

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