(4-((3-Bromophenyl)carbamoyl)phenyl)boronic acid

95%

Reagent Code: #89184
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CAS Number 874288-00-3

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scatter_plot Molecular Information
Weight 319.94634 g/mol
Formula C₁₃H₁₁BBrNO₃
badge Registry Numbers
MDL Number MFCD31648860
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronic acid reagent. Its structure, featuring a boronic acid group, enables it to form stable covalent bonds with various organic molecules, making it valuable in the construction of complex chemical structures. It is often employed in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its bromophenyl group enhances its reactivity in certain catalytic processes, allowing for precise modifications in target molecules. This chemical is also explored in medicinal chemistry for designing potential drug candidates, especially in targeting specific enzymes or receptors.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿5,562.00
inventory 250mg
10-20 days ฿22,140.00
(4-((3-Bromophenyl)carbamoyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronic acid reagent. Its structure, featuring a boronic acid group, enables it to form stable covalent bonds with various organic molecules, making it valuable in the construction of complex chemical structures. It is often employed in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its bromophenyl group enhances its reactivity in certain catalytic processes, allowing for precise modifications in target molecules. This chemical is also explored in medicinal chemistry for designing potential drug candidates, especially in targeting specific enzymes or receptors.
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