1-Isobutyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea

95%

Reagent Code: #90408
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CAS Number 874291-03-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 318.2189 g/mol
Formula C₁₇H₂₇BN₂O₃
badge Registry Numbers
MDL Number MFCD09027289
thermostat Physical Properties
Boiling Point 415.1 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.06 g/cm3
Storage 2-8°C

description Product Description

This compound is primarily used in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of biologically active molecules, particularly those targeting enzyme inhibition or receptor modulation. Its boronate ester functionality makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for constructing carbon-carbon bonds in pharmaceutical research. Additionally, it is employed in the development of proteolysis-targeting chimeras (PROTACs), which are innovative therapeutic agents designed to degrade specific disease-causing proteins. Its structural features also make it suitable for use in the preparation of boron-containing compounds, which are increasingly explored for their potential in cancer therapy and imaging applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days $120.14
inventory 1g
10-20 days $321.97
1-Isobutyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea
This compound is primarily used in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of biologically active molecules, particularly those targeting enzyme inhibition or receptor modulation. Its boronate ester functionality makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for constructing carbon-carbon bonds in pharmaceutical research. Additionally, it is employed in the development of proteolysis-targeting chimeras (PROTACs), which are innovative therapeutic agents designed to degrade specific disease-causing proteins. Its structural features also make it suitable for use in the preparation of boron-containing compounds, which are increasingly explored for their potential in cancer therapy and imaging applications.
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