[4-[(2-chloro-4-methyl-phenyl)carbamoyl]phenyl]boronic acid

98%

Reagent Code: #90360
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CAS Number 913835-39-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 289.5219 g/mol
Formula C₁₄H₁₃BClNO₃
badge Registry Numbers
MDL Number MFCD09027213
thermostat Physical Properties
Melting Point 234-236 °C
inventory_2 Storage & Handling
Density 1.34 g/cm3
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent. It facilitates the formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its application is also seen in the development of advanced materials, such as polymers and liquid crystals, where precise molecular structures are crucial. Additionally, it is employed in medicinal chemistry research for the design and synthesis of potential drug candidates, especially in the development of enzyme inhibitors and receptor modulators. Its role in these areas highlights its importance in creating innovative compounds with specific biological activities.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days $53.11
inventory 1g
10-20 days $35.41
[4-[(2-chloro-4-methyl-phenyl)carbamoyl]phenyl]boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent. It facilitates the formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its application is also seen in the development of advanced materials, such as polymers and liquid crystals, where precise molecular structures are crucial. Additionally, it is employed in medicinal chemistry research for the design and synthesis of potential drug candidates, especially in the development of enzyme inhibitors and receptor modulators. Its role in these areas highlights its importance in creating innovative compounds with specific biological activities.
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