4-Butoxyphenylboronic acid

98%

Reagent Code: #90580
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Alias 4-n-butoxyphenylboronic acid
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CAS Number 105365-51-3

science Other reagents with same CAS 105365-51-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 194.04 g/mol
Formula C₁₀H₁₅BO₃
badge Registry Numbers
MDL Number MFCD03427054
thermostat Physical Properties
Melting Point 106-108 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

4-Butoxyphenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, facilitating the coupling of aryl or vinyl halides with aryl or vinyl boronic acids. Additionally, it is employed in the development of sensors and diagnostic tools due to its ability to interact with diols and sugars, making it useful in glucose sensing and other biochemical applications. Its stability and reactivity make it a valuable compound in both industrial and research settings.

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Test Parameter Specification
Melting point 106-108
Purity (GC) 98-100
Appearance White to off-white powder
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿12,260.00
inventory 200mg
10-20 days ฿280.00
inventory 1g
10-20 days ฿960.00
inventory 5g
10-20 days ฿2,780.00

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4-Butoxyphenylboronic acid
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4-Butoxyphenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, facilitating the coupling of aryl or vinyl halides with aryl or vinyl boronic acids. Additionally, it is employed in the development of sensors and diagnostic

4-Butoxyphenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, facilitating the coupling of aryl or vinyl halides with aryl or vinyl boronic acids. Additionally, it is employed in the development of sensors and diagnostic tools due to its ability to interact with diols and sugars, making it useful in glucose sensing and other biochemical applications. Its stability and reactivity make it a valuable compound in both industrial and research settings.

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