(5-Methylfuran-2-yl)boronic acid

97%

Reagent Code: #90918
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CAS Number 62306-79-0

science Other reagents with same CAS 62306-79-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 125.92 g/mol
Formula C₅H₇BO₃
badge Registry Numbers
MDL Number MFCD01114644
thermostat Physical Properties
Boiling Point 264.4°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

(5-Methylfuran-2-yl)boronic 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. The compound serves as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and polymers. Its stability and reactivity make it a preferred choice in catalytic processes, enabling the efficient construction of diverse chemical structures. Additionally, it is utilized in the development of sensors and catalysts due to its unique boronic acid functionality, which can interact with diols and other functional groups.

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Test Parameter Specification
Purity 97-100
Melting Point 75-85
Appearance White to pale yellow powder

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿760.00
inventory 1g
10-20 days ฿2,560.00
inventory 5g
10-20 days ฿8,030.00

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(5-Methylfuran-2-yl)boronic acid
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(5-Methylfuran-2-yl)boronic 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. The compound serves as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and polymers. Its stability and reactivity make it a preferred choice in catalytic processes, enabling the

(5-Methylfuran-2-yl)boronic 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. The compound serves as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and polymers. Its stability and reactivity make it a preferred choice in catalytic processes, enabling the efficient construction of diverse chemical structures. Additionally, it is utilized in the development of sensors and catalysts due to its unique boronic acid functionality, which can interact with diols and other functional groups.

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