1-Ethyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea
98%
Reagent
Code: #90404
CAS Number
874291-00-6
blur_circular Chemical Specifications
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Molecular Information
Weight
290.1657 g/mol
Formula
C₁₅H₂₃BN₂O₃
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Registry Numbers
MDL Number
MFCD08689523
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Physical Properties
Melting Point
194-196 °C
Boiling Point
392.4 °C at 760 mmHg
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Storage & Handling
Density
1.09 g/cm3
Storage
2-8°C
description Product Description
This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, it serves as an intermediate in the production of biologically active compounds, including potential drug candidates targeting various diseases. Its structural features also make it suitable for use in materials science, particularly in the creation of advanced polymers and coatings with specific properties.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | off-white solid |
Purity | 97.5-100 |
Infrared Spectrum | Conforms to Structure |
NMR | Conforms to Structure |
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1-Ethyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea
This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, it serves as an intermediate in the production of biologically active compounds, including potential drug candidates targeting various diseases. Its structural features also make it suitable for use in materials science, particularly in the creation of advanced polymers and coatings with specific properties.
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