9,9-Di-n-octylfluorene-2,7-diboronic acid bis(pinacol) ester
98%
Reagent
Code: #94150
Alias
9,9-Dioctylfluorene-2,7-diboronic acid pinacol ester; 2,7-bis(4,4,5,5-tetramethyl-1,3-dioxo-2-boryl )-9,9-dioctylfluorene; 2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9,9 -Di-n-octylfluorene; 9,9-Di-n-octylfluorene-2,7-diboronic acid dipinacid;
CAS Number
196207-58-6
blur_circular Chemical Specifications
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Molecular Information
Weight
642.57 g/mol
Formula
C₄₁H₆₄B₂O₄
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Registry Numbers
MDL Number
MFCD16294554
thermostat
Physical Properties
Melting Point
129ºC
Boiling Point
701.622ºC at 760 mmHg
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Storage & Handling
Density
1.01g/cm3
Storage
Room temperature, dry, sealed
description Product Description
This compound is widely used in organic electronics, particularly in the synthesis of conjugated polymers for organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its structure allows it to act as a key monomer in Suzuki-Miyaura cross-coupling reactions, facilitating the creation of high-performance materials with excellent charge transport properties. Additionally, it is employed in the development of sensors and optoelectronic devices due to its ability to form stable and efficient π-conjugated systems. Its solubility in organic solvents also makes it suitable for solution-processing techniques, which are essential for large-scale manufacturing of flexible electronic devices.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | White to off-white crystal or powder |
Purity | 97.5-100 |
Infrared Spectrum | Conforms to Structure |
NMR | Conforms to Structure |
shopping_cart Available Sizes & Pricing
9,9-Di-n-octylfluorene-2,7-diboronic acid bis(pinacol) ester
This compound is widely used in organic electronics, particularly in the synthesis of conjugated polymers for organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its structure allows it to act as a key monomer in Suzuki-Miyaura cross-coupling reactions, facilitating the creation of high-performance materials with excellent charge transport properties. Additionally, it is employed in the development of sensors and optoelectronic devices due to its ability to form stable and efficient π-conjugated systems. Its solubility in organic solvents also makes it suitable for solution-processing techniques, which are essential for large-scale manufacturing of flexible electronic devices.
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