Bis(pinacolato)diboron

99%

Reagent Code: #142841
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CAS Number 73183-34-3

science Other reagents with same CAS 73183-34-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 253.94 g/mol
Formula C₁₂H₂₄B₂O₄
badge Registry Numbers
MDL Number MFCD00799570
thermostat Physical Properties
Melting Point 137-140 °C(lit.)
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Widely used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds. It serves as a source of boron, transferring boronate groups to organic substrates under mild conditions. Commonly applied in the preparation of biaryl compounds, which are important in pharmaceuticals, agrochemicals, and materials science. Its stability and ease of handling make it a preferred reagent in both academic and industrial research settings. Also used in borylation reactions to modify heteroarenes and alkenes, expanding access to functionalized building blocks for drug discovery and advanced materials.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿920.00
5g
10-20 days ฿2,160.00
25g
10-20 days ฿4,220.00
100g
10-20 days ฿12,050.00
Bis(pinacolato)diboron
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Widely used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds. It serves as a source of boron, transferring boronate groups to organic substrates under mild conditions. Commonly applied in the preparation of biaryl compounds, which are important in pharmaceuticals, agrochemicals, and materials science. Its stability and ease of handling make it a preferred reagent in both academic and industrial research setti

Widely used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds. It serves as a source of boron, transferring boronate groups to organic substrates under mild conditions. Commonly applied in the preparation of biaryl compounds, which are important in pharmaceuticals, agrochemicals, and materials science. Its stability and ease of handling make it a preferred reagent in both academic and industrial research settings. Also used in borylation reactions to modify heteroarenes and alkenes, expanding access to functionalized building blocks for drug discovery and advanced materials.

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