(E)-(2-Cyclopentylvinyl)boronic acid

96%, contains TBC as stabilizer

Reagent Code: #181094
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CAS Number 161282-93-5

science Other reagents with same CAS 161282-93-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 139.99 g/mol
Formula C₇H₁₃BO₂
badge Registry Numbers
MDL Number MFCD09840294
thermostat Physical Properties
Melting Point 70-72 °C
Boiling Point 266.1±23.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.119±0.06 g/cm3(Predicted)
Storage -20°C, Sealed, Inert Gas

description Product Description

Used in organic synthesis as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its vinylboronic acid structure allows for the introduction of cyclopentylvinyl groups into aromatic or heteroaromatic systems, which is valuable in the development of pharmaceuticals and agrochemicals. The (E)-configuration ensures stereochemical control in the resulting olefin products, making it useful in the synthesis of complex molecules where specific geometry is required. Also employed in medicinal chemistry for building blocks in drug discovery due to its stability and reactivity profile.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿5,660.00
inventory 100mg
10-20 days ฿9,650.00
inventory 250mg
10-20 days ฿16,430.00

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(E)-(2-Cyclopentylvinyl)boronic acid
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Used in organic synthesis as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its vinylboronic acid structure allows for the introduction of cyclopentylvinyl groups into aromatic or heteroaromatic systems, which is valuable in the development of pharmaceuticals and agrochemicals. The (E)-configuration ensures stereochemical control in the resulting olefin products, making it useful in the synthesis of complex molecules where specific geometry is req

Used in organic synthesis as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its vinylboronic acid structure allows for the introduction of cyclopentylvinyl groups into aromatic or heteroaromatic systems, which is valuable in the development of pharmaceuticals and agrochemicals. The (E)-configuration ensures stereochemical control in the resulting olefin products, making it useful in the synthesis of complex molecules where specific geometry is required. Also employed in medicinal chemistry for building blocks in drug discovery due to its stability and reactivity profile.

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