(5-Fluoro-2-(N-methylsulfamoyl)phenyl)boronic acid

98%

Reagent Code: #186485
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CAS Number 1218790-75-0

science Other reagents with same CAS 1218790-75-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.03 g/mol
Formula C₇H₉BFNO₄S
badge Registry Numbers
MDL Number MFCD15143479
thermostat Physical Properties
Boiling Point 432.2±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.49±0.1 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. It plays an important role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in drug discovery processes. Commonly utilized in the preparation of potential sulfonyl-containing therapeutic agents, including those investigated for anticancer and anti-inflammatory activities. Its boronic acid group facilitates palladium-catalyzed coupling, making it valuable in medicinal chemistry for constructing complex aromatic frameworks.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,090.00
inventory 1g
10-20 days ฿11,010.00
inventory 5g
10-20 days ฿44,000.00
(5-Fluoro-2-(N-methylsulfamoyl)phenyl)boronic acid
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. It plays an important role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in drug discovery processes. Commonly utilized in the preparation of potential sulfonyl-containing therapeutic agents, including those investigated for anticancer and anti-inflammatory activities. Its boronic acid group facilitates palladium-catalyzed coupling, making it valuable in medicinal chemistry for constructing complex aromatic frameworks.
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