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

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Reagent Code: #165273
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CAS Number 957120-51-3

science Other reagents with same CAS 957120-51-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.4 g/mol
Formula C₈H₉BClNO₃
badge Registry Numbers
MDL Number MFCD09800856
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 kinase inhibitors for cancer treatment. Its boronic acid functional group enables Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing biaryl structures common in drug molecules. Also applied in the preparation of covalent inhibitors due to the ability of boronic acids to form reversible bonds with biological nucleophiles like serine residues in enzymes. Commonly employed in medicinal chemistry research for lead optimization and library synthesis in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,840.00

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(3-Chloro-5-(methylcarbamoyl)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 kinase inhibitors for cancer treatment. Its boronic acid functional group enables Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing biaryl structures common in drug molecules. Also applied in the preparation of covalent inhibitors due to the ability of boronic acids to form reversible bonds with biological nucleophiles like serine residues in enzyme

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and kinase inhibitors for cancer treatment. Its boronic acid functional group enables Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing biaryl structures common in drug molecules. Also applied in the preparation of covalent inhibitors due to the ability of boronic acids to form reversible bonds with biological nucleophiles like serine residues in enzymes. Commonly employed in medicinal chemistry research for lead optimization and library synthesis in drug discovery programs.

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