(4-(N-(4-Methoxybenzyl)-N-methylsulfamoyl)phenyl)boronic acid

98%

Reagent Code: #215680
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CAS Number 913835-54-8

science Other reagents with same CAS 913835-54-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 335.18 g/mol
Formula C₁₅H₁₈BNO₅S
badge Registry Numbers
MDL Number MFCD08689488
thermostat Physical Properties
Melting Point 137-139 °C
Boiling Point 545.2±60.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.35±0.1 g/cm3(Predicted)
Storage Room temperature, seal, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing biaryl structures commonly found in bioactive molecules. Also employed in the preparation of proteasome inhibitors due to the ability of boronic acids to reversibly bind serine residues in enzyme active sites. Widely applied in medicinal chemistry for lead optimization and in the creation of targeted therapies for oncology and inflammatory diseases.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,440.00
inventory 5g
10-20 days ฿11,260.00

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(4-(N-(4-Methoxybenzyl)-N-methylsulfamoyl)phenyl)boronic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing biaryl structures commonly found in bioactive molecules. Also employed in the preparation of proteasome inhibitors due to the ability of boronic acids to reversibly bind serine residues in enzyme active sites. Widely applied in m

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing biaryl structures commonly found in bioactive molecules. Also employed in the preparation of proteasome inhibitors due to the ability of boronic acids to reversibly bind serine residues in enzyme active sites. Widely applied in medicinal chemistry for lead optimization and in the creation of targeted therapies for oncology and inflammatory diseases.

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