2,6-Diisopropylphenylboronic Acid

≥95%

Reagent Code: #89583
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CAS Number 363166-79-4

science Other reagents with same CAS 363166-79-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.09 g/mol
Formula C₁₂H₁₉O₂B
badge Registry Numbers
MDL Number MFCD16876786
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

2,6-Diisopropylphenylboronic 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 acts as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and polymers. Its sterically hindered structure enhances selectivity in catalytic processes, making it a preferred choice for specific transformations. Additionally, it is employed in the development of sensors and catalysts due to its ability to interact with various functional groups.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿1,449.00
inventory 1g
10-20 days ฿5,778.00
inventory 5g
10-20 days ฿20,709.00
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2,6-Diisopropylphenylboronic Acid
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2,6-Diisopropylphenylboronic 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 acts as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and polymers. Its sterically hindered structure enhances selectivity in catalytic processes, making it a pre

2,6-Diisopropylphenylboronic 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 acts as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and polymers. Its sterically hindered structure enhances selectivity in catalytic processes, making it a preferred choice for specific transformations. Additionally, it is employed in the development of sensors and catalysts due to its ability to interact with various functional groups.

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