(2-(Diethylcarbamoyl)phenyl)boronic acid

95%

Reagent Code: #215881
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CAS Number 129112-21-6

science Other reagents with same CAS 129112-21-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.06 g/mol
Formula C₁₁H₁₆BNO₃
badge Registry Numbers
MDL Number MFCD01318988
thermostat Physical Properties
Melting Point 64-70 °C
Boiling Point 432.0±47.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.14±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic acid functionality enables efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of bioactive compounds and functional materials where precise molecular architecture is required. The presence of a diethylcarbamoyl group enhances solubility and can influence reactivity and selectivity in coupling processes.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿2,800.00
250mg
10-20 days ฿4,640.00
1g
10-20 days ฿12,540.00
(2-(Diethylcarbamoyl)phenyl)boronic acid
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic acid functionality enables efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of bioactive compounds and functional materials where precise molecular architecture is required. The presence of a diethylcarbamoyl group enhances solubility and can influence reactivity and sel

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic acid functionality enables efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of bioactive compounds and functional materials where precise molecular architecture is required. The presence of a diethylcarbamoyl group enhances solubility and can influence reactivity and selectivity in coupling processes.

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