2-(7-Bromo-9,9-di-n-octyl-9H-fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

98%

Reagent Code: #64190
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CAS Number 620624-96-6

science Other reagents with same CAS 620624-96-6

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Weight 595.51 g/mol
Formula C₃₅H₅₂BBrO₂
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This chemical is primarily utilized in the field of organic electronics, particularly in the synthesis of organic semiconductors. Its structure, featuring a fluorene core and a boronate ester group, makes it a valuable building block for creating conjugated polymers and small molecules. These materials are essential for developing organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and organic field-effect transistors (OFETs). The compound's ability to participate in Suzuki-Miyaura cross-coupling reactions allows for the precise construction of complex organic frameworks, enhancing the performance and efficiency of electronic devices. Additionally, its solubility in common organic solvents facilitates processing in solution-based fabrication techniques, which are critical for large-scale production of flexible and lightweight electronic components.

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inventory 50mg
10-20 days ฿16,690.00

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2-(7-Bromo-9,9-di-n-octyl-9H-fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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This chemical is primarily utilized in the field of organic electronics, particularly in the synthesis of organic semiconductors. Its structure, featuring a fluorene core and a boronate ester group, makes it a valuable building block for creating conjugated polymers and small molecules. These materials are essential for developing organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and organic field-effect transistors (OFETs). The compound's ability to participate in Suzuki-Miyaura cross

This chemical is primarily utilized in the field of organic electronics, particularly in the synthesis of organic semiconductors. Its structure, featuring a fluorene core and a boronate ester group, makes it a valuable building block for creating conjugated polymers and small molecules. These materials are essential for developing organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and organic field-effect transistors (OFETs). The compound's ability to participate in Suzuki-Miyaura cross-coupling reactions allows for the precise construction of complex organic frameworks, enhancing the performance and efficiency of electronic devices. Additionally, its solubility in common organic solvents facilitates processing in solution-based fabrication techniques, which are critical for large-scale production of flexible and lightweight electronic components.

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