Thiophene-2,5-diboronic acid bis(pinacol) ester

98%

Reagent Code: #91128
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CAS Number 175361-81-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 336.06 g/mol
Formula C₁₆H₂₆B₂O₄S
thermostat Physical Properties
Melting Point 227-231°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is widely used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It facilitates the formation of carbon-carbon bonds, enabling the construction of complex organic molecules, including pharmaceuticals, agrochemicals, and functional materials. Its boronic ester groups are highly reactive with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable for producing conjugated systems like thiophene-based polymers. These polymers are essential in organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs), due to their excellent charge transport properties. Additionally, it is employed in the development of sensors and ligands for catalysis, leveraging its stability and reactivity under mild conditions.

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Test Parameter Specification
Appearance White - very pale yellow : Crystal - powder
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days £23.77
inventory 5g
10-20 days £84.56
Thiophene-2,5-diboronic acid bis(pinacol) ester
This compound is widely used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It facilitates the formation of carbon-carbon bonds, enabling the construction of complex organic molecules, including pharmaceuticals, agrochemicals, and functional materials. Its boronic ester groups are highly reactive with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable for producing conjugated systems like thiophene-based polymers. These polymers are essential in organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs), due to their excellent charge transport properties. Additionally, it is employed in the development of sensors and ligands for catalysis, leveraging its stability and reactivity under mild conditions.
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