1-Propyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea
95%
Reagent
Code: #90403
CAS Number
874291-01-7
blur_circular Chemical Specifications
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Molecular Information
Weight
304.1923 g/mol
Formula
C₁₆H₂₅BN₂O₃
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Registry Numbers
MDL Number
MFCD09027288
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Physical Properties
Melting Point
225-228 °C
Boiling Point
406.3 °C at 760 mmHg
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Storage & Handling
Density
1.07 g/cm3
Storage
2-8°C
description Product Description
This compound is primarily used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the preparation of boron-containing compounds, which are valuable in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed to create complex organic molecules, including drugs and biologically active compounds. Additionally, its urea moiety can contribute to hydrogen bonding interactions, making it useful in the design of molecules with specific binding properties, such as enzyme inhibitors or receptor modulators. Its boronate ester group also allows for further functionalization, enabling the synthesis of diverse chemical structures.
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1-Propyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea
This compound is primarily used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the preparation of boron-containing compounds, which are valuable in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed to create complex organic molecules, including drugs and biologically active compounds. Additionally, its urea moiety can contribute to hydrogen bonding interactions, making it useful in the design of molecules with specific binding properties, such as enzyme inhibitors or receptor modulators. Its boronate ester group also allows for further functionalization, enabling the synthesis of diverse chemical structures.
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