2,​2'-​(9,​9'-​spirobi[9H-​fluorene]​-​2,​7-​diyl)​bis[4,​4,​5,​5-​tetramethyl-1,​3,​2-​Dioxaborolane

98%

Reagent Code: #94386
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CAS Number 728911-52-2

science Other reagents with same CAS 728911-52-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 568.3200000000001 g/mol
Formula C₃₇H₃₈B₂O₄
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its spirobifluorene structure provides rigidity and stability, making it valuable in the development of organic electronic materials. It is often employed in the synthesis of conjugated polymers and small molecules for applications in organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). The dioxaborolane groups act as key functional units, enabling efficient boron-based coupling reactions to construct complex organic frameworks. Additionally, its unique structure contributes to enhancing the thermal and morphological stability of the resulting materials, which is crucial for high-performance electronic devices.

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Test Parameter Specification
Appearance White to slightly pale yellow crystal-powder solid
Purity 97.5-100%
Proton NMR Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿720.00
inventory 1g
10-20 days ฿2,370.00
inventory 5g
10-20 days ฿8,350.00

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2,​2'-​(9,​9'-​spirobi[9H-​fluorene]​-​2,​7-​diyl)​bis[4,​4,​5,​5-​tetramethyl-1,​3,​2-​Dioxaborolane
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This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its spirobifluorene structure provides rigidity and stability, making it valuable in the development of organic electronic materials. It is often employed in the synthesis of conjugated polymers and small molecules for applications in organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). The dioxaborolane groups act as key functional units, enabling efficient boron-based coupling reactions to construct complex organic frameworks. Additionally, its unique structure contributes to enhancing the thermal and morphological stability of the resulting materials, which is crucial for high-performance electronic devices.
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