(E)-3,3-dimethylbut-1-enylboronic acid

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Reagent Code: #184534
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CAS Number 86595-37-1

science Other reagents with same CAS 86595-37-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 127.98 g/mol
Formula C₆H₁₃BO₂
badge Registry Numbers
MDL Number MFCD01074624
thermostat Physical Properties
Melting Point 78-80 °C
Boiling Point 212.4±23.0 °C(Predicted)
inventory_2 Storage & Handling
Density 0.926±0.06 g/cm3(Predicted)
Storage -20°C, Inert Gas

description Product Description

Used in organic synthesis as a boronic acid coupling partner in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its vinylboronic acid structure with a geminal dimethyl group enhances stability and influences stereoselectivity in coupling processes. Commonly employed in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals, where controlled alkene incorporation is required. The (E)-configuration ensures defined geometry in the resulting coupled products, which is critical for desired biological activity or material properties. Also useful in conjugation strategies for modifying small molecules in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,340.00
inventory 1g
10-20 days ฿6,160.00
inventory 5g
10-20 days ฿21,730.00
inventory 25g
10-20 days ฿72,000.00
inventory 100g
10-20 days ฿224,000.00

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(E)-3,3-dimethylbut-1-enylboronic acid
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Used in organic synthesis as a boronic acid coupling partner in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its vinylboronic acid structure with a geminal dimethyl group enhances stability and influences stereoselectivity in coupling processes. Commonly employed in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals, where controlled alkene incorporation is required. The (E)-configuration ensures defined geometry in the resul

Used in organic synthesis as a boronic acid coupling partner in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its vinylboronic acid structure with a geminal dimethyl group enhances stability and influences stereoselectivity in coupling processes. Commonly employed in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals, where controlled alkene incorporation is required. The (E)-configuration ensures defined geometry in the resulting coupled products, which is critical for desired biological activity or material properties. Also useful in conjugation strategies for modifying small molecules in medicinal chemistry.

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