9,9-Di-n-octylfluorene-2,7-diboronic acid bis(pinacol) ester

98%

Reagent Code: #94150
label
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;
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CAS Number 196207-58-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 642.57 g/mol
Formula C₄₁H₆₄B₂O₄
badge Registry Numbers
MDL Number MFCD16294554
thermostat Physical Properties
Melting Point 129ºC
Boiling Point 701.622ºC at 760 mmHg
inventory_2 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

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿820.00
inventory 5g
10-20 days ฿3,060.00
inventory 25g
10-20 days ฿11,990.00
inventory 100g
10-20 days ฿44,660.00
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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