5-(4-Tolyl)thiophene-2-boronic acid pinacol ester

95%

Reagent Code: #90814
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CAS Number 2223031-94-3

science Other reagents with same CAS 2223031-94-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 318.23872 g/mol
Formula C₁₇H₂₃BO₃S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. The boronic ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in drug discovery and material science. Additionally, it is employed in the production of organic electronic materials, such as polymers and small molecules, for use in OLEDs and other optoelectronic devices. Its stability and reactivity make it a valuable tool in modern synthetic chemistry.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿8,982.00
inventory 25mg
10-20 days ฿19,800.00

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5-(4-Tolyl)thiophene-2-boronic acid pinacol ester
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This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. The boronic ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in drug discovery and material science. Additionally, it is employed in the production of organic electronic materia

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. The boronic ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in drug discovery and material science. Additionally, it is employed in the production of organic electronic materials, such as polymers and small molecules, for use in OLEDs and other optoelectronic devices. Its stability and reactivity make it a valuable tool in modern synthetic chemistry.

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