(3-(Methoxycarbonyl)-4-methylphenyl)boronic acid

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Reagent Code: #119427
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CAS Number 1048330-10-4

science Other reagents with same CAS 1048330-10-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.99 g/mol
Formula C₉H₁₁BO₄
badge Registry Numbers
MDL Number MFCD13191800
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It acts as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in constructing complex molecular structures. Additionally, it is employed in the development of sensors and imaging agents due to its ability to interact with specific biological targets. Its applications also extend to research in medicinal chemistry, where it is used to design and synthesize novel drug candidates.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,076.00
inventory 100mg
10-20 days ฿1,179.00
inventory 250mg
10-20 days ฿2,007.00
inventory 5g
10-20 days ฿22,194.00

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(3-(Methoxycarbonyl)-4-methylphenyl)boronic acid
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This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It acts as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in constructing complex molecular structures. Additionally, it is employed in the development of sensors and imaging agents due to its ability to interact with specific biologica

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It acts as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in constructing complex molecular structures. Additionally, it is employed in the development of sensors and imaging agents due to its ability to interact with specific biological targets. Its applications also extend to research in medicinal chemistry, where it is used to design and synthesize novel drug candidates.

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