(3-Amino-5-(methoxycarbonyl)phenyl)boronic acid

98%

Reagent Code: #139021
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CAS Number 380430-56-8

science Other reagents with same CAS 380430-56-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 194.98 g/mol
Formula C₈H₁₀BNO₄
badge Registry Numbers
MDL Number MFCD02179467
thermostat Physical Properties
Melting Point 220-226 °C
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Dry, Light-proof, Inert Gas

description Product Description

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, 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 and development. The presence of both amino and ester functional groups allows for further chemical modifications, enhancing its utility in creating complex molecules. Commonly employed in the synthesis of bioactive compounds and functional materials.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿4,030.00
1g
10-20 days ฿10,840.00
5g
10-20 days ฿44,410.00
(3-Amino-5-(methoxycarbonyl)phenyl)boronic acid
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Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, 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 and development. The presence of both amino and ester functional groups allows for further chemical modifications, enhancing its utility in creating complex molecules. Commonly employed in the synthesis of bioactive compounds and func

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, 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 and development. The presence of both amino and ester functional groups allows for further chemical modifications, enhancing its utility in creating complex molecules. Commonly employed in the synthesis of bioactive compounds and functional materials.

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