(3-(3-Ethoxy-3-oxopropyl)phenyl)boronic acid

98%

Reagent Code: #90111
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CAS Number 913835-82-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.05 g/mol
Formula C₁₁H₁₅BO₄
badge Registry Numbers
MDL Number MFCD08689511
thermostat Physical Properties
Melting Point 94-96°C
Boiling Point 382.6°C
inventory_2 Storage & Handling
Density 1.15g/mL
Storage  2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group acts as a key functional group, enabling the formation of carbon-carbon bonds, which is essential in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it serves as a building block in the development of advanced materials, such as polymers and sensors, due to its ability to interact with diols and other functional groups. Its ethoxy group further enhances its solubility and reactivity in various organic solvents, making it a versatile reagent in chemical research and industrial applications.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days $398.78
(3-(3-Ethoxy-3-oxopropyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group acts as a key functional group, enabling the formation of carbon-carbon bonds, which is essential in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it serves as a building block in the development of advanced materials, such as polymers and sensors, due to its ability to interact with diols and other functional groups. Its ethoxy group further enhances its solubility and reactivity in various organic solvents, making it a versatile reagent in chemical research and industrial applications.
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