(4-((2-Methoxyphenyl)carbamoyl)phenyl)boronic acid

98%

Reagent Code: #89181
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CAS Number 1704069-56-6

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scatter_plot Molecular Information
Weight 271.08 g/mol
Formula C₁₄H₁₄BNO₄
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MDL Number MFCD28384306
inventory_2 Storage & Handling
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 to form carbon-carbon bonds. Its structure, featuring a methoxyphenyl group, enhances its reactivity and selectivity in these reactions, making it valuable for constructing complex organic molecules, such as pharmaceuticals and advanced materials. Additionally, its boronic acid moiety allows it to interact with diols and other Lewis bases, enabling its use in sensor development and biochemical applications, such as glucose sensing or protein labeling. The compound’s stability and compatibility with various reaction conditions further broaden its utility in medicinal chemistry and material science.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿36,640.00
(4-((2-Methoxyphenyl)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 to form carbon-carbon bonds. Its structure, featuring a methoxyphenyl group, enhances its reactivity and selectivity in these reactions, making it valuable for constructing complex organic molecules, such as pharmaceuticals and advanced materials. Additionally, its boronic acid moiety allows it to interact with diols and other Lewis bases, enabling its use in sensor development and biochemical applications, such as glucose sensing or protein labeling. The compound’s stability and compatibility with various reaction conditions further broaden its utility in medicinal chemistry and material science.
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