3-Chloro-4-(N-isopropylcarbamoyl)phenylboronic acid

98%

Reagent Code: #164747
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CAS Number 850589-41-2

science Other reagents with same CAS 850589-41-2

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Weight 241.5 g/mol
Formula C₁₀H₁₃BClNO₃
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MDL Number MFCD07363768
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Storage Room temperature

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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. Its boronic acid functional group enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing complex organic molecules for drug discovery. Commonly employed in the preparation of bioactive molecules targeting diseases such as diabetes, cancer, and inflammatory conditions. Also utilized in the design of covalent inhibitors due to the reactivity of the boronic acid moiety with serine residues in enzyme active sites.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,940.00

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3-Chloro-4-(N-isopropylcarbamoyl)phenylboronic 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. Its boronic acid functional group enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing complex organic molecules for drug discovery. Commonly employed in the preparation of bioactive molecules targeting diseases such as diabetes, cancer, and inflammatory conditions. Also utilized in the design of covalent inh

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and kinase inhibitors. Its boronic acid functional group enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing complex organic molecules for drug discovery. Commonly employed in the preparation of bioactive molecules targeting diseases such as diabetes, cancer, and inflammatory conditions. Also utilized in the design of covalent inhibitors due to the reactivity of the boronic acid moiety with serine residues in enzyme active sites.

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