[4-(3-ethoxy-3-oxopropyl)phenyl]boronic acid
98%
Reagent
Code: #90405
CAS Number
660440-57-3
blur_circular Chemical Specifications
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Molecular Information
Weight
222.04 g/mol
Formula
C₁₁H₁₅BO₄
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Registry Numbers
MDL Number
MFCD04115652
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Physical Properties
Melting Point
80-84°C
Boiling Point
370.7°C
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Storage & Handling
Density
1.15g/mL
Storage
2-8°C
description Product Description
This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of sensors and probes due to its ability to interact with diols and other functional groups, making it useful in biochemical and analytical applications.
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[4-(3-ethoxy-3-oxopropyl)phenyl]boronic acid
This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of sensors and probes due to its ability to interact with diols and other functional groups, making it useful in biochemical and analytical applications.
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