4,4,5,5-tetramethyl-2-(4-2-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethynylphenyl)-1,3,2-dioxaborolane

95%

Reagent Code: #118389
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CAS Number 849681-64-7

science Other reagents with same CAS 849681-64-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 430.16 g/mol
Formula C₂₆H₃₂B₂O₄
badge Registry Numbers
MDL Number MFCD16294524
thermostat Physical Properties
Melting Point 275-280 °C
inventory_2 Storage & Handling
Storage Room temperature, airtight, dry

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its structure, featuring two boronate ester groups, makes it a valuable intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and advanced materials. The compound is also employed in the synthesis of conjugated polymers and small molecules for organic electronics, including organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its stability and reactivity under mild conditions make it a preferred choice for borylation reactions, enabling the efficient introduction of boron-containing functional groups into target molecules.

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Test Parameter Specification
Appearance Solid
Purity (%) 94.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,200.00

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4,4,5,5-tetramethyl-2-(4-2-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethynylphenyl)-1,3,2-dioxaborolane
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This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its structure, featuring two boronate ester groups, makes it a valuable intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and advanced materials. The compound is also employed in the synthesis of conjugated polymers and small molecules for organic electronics, including organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its stability and reactivity under mild conditions make it a preferred choice for borylation reactions, enabling the efficient introduction of boron-containing functional groups into target molecules.
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