3-Methoxy-4-(methoxycarbonyl)phenylboronic acid

98%

Reagent Code: #90247
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CAS Number 603122-41-4

science Other reagents with same CAS 603122-41-4

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scatter_plot Molecular Information
Weight 209.99 g/mol
Formula C₉H₁₁BO₅
badge Registry Numbers
MDL Number MFCD07366483
inventory_2 Storage & Handling
Storage 2~8℃, inert gas atmosphere

description Product Description

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for creating complex organic molecules, often in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in constructing biologically active compounds. Additionally, it is utilized in material science for the synthesis of advanced polymers and functional materials. Its methoxy and methoxycarbonyl groups contribute to its reactivity and stability, allowing for precise control in synthetic processes.

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Test Parameter Specification
Purity 97.5-100%

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,683.00
inventory 5g
10-20 days ฿7,740.00
inventory 25g
10-20 days ฿34,911.00

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3-Methoxy-4-(methoxycarbonyl)phenylboronic acid
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This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for creating complex organic molecules, often in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in constructing biologically active compounds. Additionally, it is utilized in material science for the synthesis of advanced polymers and functional ma

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for creating complex organic molecules, often in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in constructing biologically active compounds. Additionally, it is utilized in material science for the synthesis of advanced polymers and functional materials. Its methoxy and methoxycarbonyl groups contribute to its reactivity and stability, allowing for precise control in synthetic processes.

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