(3-Chloro-5-(diethylcarbamoyl)phenyl)boronic acid

98%

Reagent Code: #165275
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CAS Number 957120-59-1

science Other reagents with same CAS 957120-59-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.5 g/mol
Formula C₁₁H₁₅BClNO₃
badge Registry Numbers
MDL Number MFCD09800862
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its boronic acid functional group enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in medicinal chemistry for constructing carbon-carbon bonds. Commonly employed in research settings to design enzyme inhibitors, especially targeting serine proteases involved in disease pathways. Also utilized in the preparation of boron-containing compounds for potential use in neutron capture therapy and molecular imaging.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,820.00
inventory 250mg
10-20 days ฿3,100.00
inventory 1g
10-20 days ฿8,340.00
inventory 5g
10-20 days ฿29,200.00

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(3-Chloro-5-(diethylcarbamoyl)phenyl)boronic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its boronic acid functional group enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in medicinal chemistry for constructing carbon-carbon bonds. Commonly employed in research settings to design enzyme inhibitors, especially targeting serine proteases involved in disease pathways. Also utilized in the preparation o

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its boronic acid functional group enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in medicinal chemistry for constructing carbon-carbon bonds. Commonly employed in research settings to design enzyme inhibitors, especially targeting serine proteases involved in disease pathways. Also utilized in the preparation of boron-containing compounds for potential use in neutron capture therapy and molecular imaging.

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