2-Cyano-3-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxa-borolan-2-yl)-phenyl]-acrylic acid ethyl ester

95%

Reagent Code: #116578
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CAS Number 1218790-51-2

science Other reagents with same CAS 1218790-51-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 327.18 g/mol
Formula C₁₈H₂₂BNO₄
badge Registry Numbers
MDL Number MFCD11113044
thermostat Physical Properties
Melting Point 104-108 °C
inventory_2 Storage & Handling
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description Product Description

This compound is primarily utilized in organic synthesis, particularly in the preparation of advanced materials and functional molecules. It serves as a key intermediate in the development of organic semiconductors and photovoltaic materials due to its electron-accepting properties and ability to form stable conjugated systems. The compound is also employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, to construct complex organic frameworks for use in optoelectronic devices. Additionally, its boronate ester group makes it valuable in the synthesis of polymers and small molecules for applications in organic light-emitting diodes (OLEDs) and dye-sensitized solar cells (DSSCs). Its structural features enable fine-tuning of electronic properties, making it a versatile component in materials science research.

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inventory 1g
10-20 days ฿4,374.00

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2-Cyano-3-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxa-borolan-2-yl)-phenyl]-acrylic acid ethyl ester
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This compound is primarily utilized in organic synthesis, particularly in the preparation of advanced materials and functional molecules. It serves as a key intermediate in the development of organic semiconductors and photovoltaic materials due to its electron-accepting properties and ability to form stable conjugated systems. The compound is also employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, to construct complex organic frameworks for use in optoelectronic devices. Additionally

This compound is primarily utilized in organic synthesis, particularly in the preparation of advanced materials and functional molecules. It serves as a key intermediate in the development of organic semiconductors and photovoltaic materials due to its electron-accepting properties and ability to form stable conjugated systems. The compound is also employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, to construct complex organic frameworks for use in optoelectronic devices. Additionally, its boronate ester group makes it valuable in the synthesis of polymers and small molecules for applications in organic light-emitting diodes (OLEDs) and dye-sensitized solar cells (DSSCs). Its structural features enable fine-tuning of electronic properties, making it a versatile component in materials science research.

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