3-(Ethylcarbamoyl)-5-nitrophenylboronic acid

98%

Reagent Code: #184965
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CAS Number 871332-79-5

science Other reagents with same CAS 871332-79-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 238.01 g/mol
Formula C₉H₁₁BN₂O₅
badge Registry Numbers
MDL Number MFCD07783872
thermostat Physical Properties
Melting Point 187-191 °C
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used in organic synthesis as a building block for pharmaceuticals, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its boronic acid group enables efficient carbon-carbon bond formation, making it valuable in drug discovery. The nitro and ethylcarbamoyl functional groups allow further chemical modifications, enhancing its utility in developing bioactive molecules. Commonly applied in the preparation of kinase inhibitors and other therapeutic agents where aromatic ring systems are required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,360.00
inventory 5g
10-20 days ฿25,350.00
inventory 25g
10-20 days ฿76,050.00
inventory 1g
10-20 days ฿6,340.00
3-(Ethylcarbamoyl)-5-nitrophenylboronic acid
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Used in organic synthesis as a building block for pharmaceuticals, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its boronic acid group enables efficient carbon-carbon bond formation, making it valuable in drug discovery. The nitro and ethylcarbamoyl functional groups allow further chemical modifications, enhancing its utility in developing bioactive molecules. Commonly applied in the preparation of kinase inhibitors and other therapeutic agents where aromatic ring sys

Used in organic synthesis as a building block for pharmaceuticals, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its boronic acid group enables efficient carbon-carbon bond formation, making it valuable in drug discovery. The nitro and ethylcarbamoyl functional groups allow further chemical modifications, enhancing its utility in developing bioactive molecules. Commonly applied in the preparation of kinase inhibitors and other therapeutic agents where aromatic ring systems are required.

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