4-Ethoxyphenylboronic acid

98%

Reagent Code: #90546
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Alias 4-Ethoxyphenylboronic acid
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CAS Number 22237-13-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165.98 g/mol
Formula C₈H₁₁BO₃
badge Registry Numbers
MDL Number MFCD00674028
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

4-Ethoxyphenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its role as a boronic acid derivative allows it to act as a key intermediate in the synthesis of complex organic molecules. Additionally, it is utilized in the development of sensors and molecular recognition systems due to its ability to interact with diols and other functional groups. Its applications extend to research in medicinal chemistry, where it contributes to the creation of novel drug candidates and bioactive compounds.

format_list_bulleted Product Specification

Test Parameter Specification
Purity 97.5-100
Appearance White to light yellow powder to crystal
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿280.00
inventory 5g
10-20 days ฿590.00
inventory 25g
10-20 days ฿2,050.00
inventory 100g
10-20 days ฿7,700.00
4-Ethoxyphenylboronic acid
4-Ethoxyphenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its role as a boronic acid derivative allows it to act as a key intermediate in the synthesis of complex organic molecules. Additionally, it is utilized in the development of sensors and molecular recognition systems due to its ability to interact with diols and other functional groups. Its applications extend to research in medicinal chemistry, where it contributes to the creation of novel drug candidates and bioactive compounds.
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