3-Isopropylphenylboronic acid

98%

Reagent Code: #90134
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CAS Number 216019-28-2

science Other reagents with same CAS 216019-28-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 164.01 g/mol
Formula C₉H₁₃BO₂
badge Registry Numbers
MDL Number MFCD01074634
thermostat Physical Properties
Melting Point 70-72°C
Boiling Point 294.2°C
inventory_2 Storage & Handling
Density 1.04g/mL
Storage  2-8°C

description Product Description

3-Isopropylphenylboronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form 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 active pharmaceutical ingredients (APIs) and fine chemicals. Its boronic acid group facilitates the coupling with aryl halides or pseudohalides, enabling the creation of biaryl structures, which are common in many biologically active compounds. Additionally, it is utilized in the development of sensors and catalysts due to its ability to interact with various organic and inorganic substrates.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿477.00
inventory 5g
10-20 days ฿2,223.00
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3-Isopropylphenylboronic acid
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3-Isopropylphenylboronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form 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 active pharmaceutical ingredients (APIs) and fine chemicals. Its boronic acid group facilitates the coupling with aryl halides

3-Isopropylphenylboronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form 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 active pharmaceutical ingredients (APIs) and fine chemicals. Its boronic acid group facilitates the coupling with aryl halides or pseudohalides, enabling the creation of biaryl structures, which are common in many biologically active compounds. Additionally, it is utilized in the development of sensors and catalysts due to its ability to interact with various organic and inorganic substrates.

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