(3-((3-Ethoxy-3-oxopropyl)carbamoyl)phenyl)boronic acid

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Reagent Code: #185385
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CAS Number 850567-28-1

science Other reagents with same CAS 850567-28-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.07 g/mol
Formula C₁₂H₁₆BNO₅
badge Registry Numbers
MDL Number MFCD04115701
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used in organic synthesis as a building block for pharmaceuticals and bioactive compounds. Its boronic acid group enables Suzuki-Miyaura cross-coupling reactions, making it valuable in drug development for forming carbon-carbon bonds. Commonly applied in the preparation of protease inhibitors and kinase inhibitors due to its ability to interact with biological targets. Also utilized in the synthesis of sensors and functional materials where selective binding or conjugation is required. The presence of both amide and ester functionalities allows for further chemical modifications, enhancing its versatility in medicinal chemistry and material science.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,820.00
inventory 1g
10-20 days ฿13,000.00
inventory 5g
10-20 days ฿45,500.00

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(3-((3-Ethoxy-3-oxopropyl)carbamoyl)phenyl)boronic acid
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Used in organic synthesis as a building block for pharmaceuticals and bioactive compounds. Its boronic acid group enables Suzuki-Miyaura cross-coupling reactions, making it valuable in drug development for forming carbon-carbon bonds. Commonly applied in the preparation of protease inhibitors and kinase inhibitors due to its ability to interact with biological targets. Also utilized in the synthesis of sensors and functional materials where selective binding or conjugation is required. The presence of bo

Used in organic synthesis as a building block for pharmaceuticals and bioactive compounds. Its boronic acid group enables Suzuki-Miyaura cross-coupling reactions, making it valuable in drug development for forming carbon-carbon bonds. Commonly applied in the preparation of protease inhibitors and kinase inhibitors due to its ability to interact with biological targets. Also utilized in the synthesis of sensors and functional materials where selective binding or conjugation is required. The presence of both amide and ester functionalities allows for further chemical modifications, enhancing its versatility in medicinal chemistry and material science.

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