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

95%

Reagent Code: #90409
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CAS Number 874297-80-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 330.2296 g/mol
Formula C₁₈H₂₇BN₂O₃
badge Registry Numbers
MDL Number MFCD09027290
thermostat Physical Properties
Boiling Point 444.1 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.11 g/cm3
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis and medicinal chemistry as a key intermediate in the development of boron-containing molecules. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and organic materials. Additionally, its urea moiety can contribute to hydrogen bonding interactions, making it useful in the design of enzyme inhibitors or receptor ligands. The compound is often explored in drug discovery for its potential to enhance binding affinity and selectivity in target molecules. Its stability and reactivity also make it suitable for use in bioconjugation and labeling applications in chemical biology.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days $236.96
inventory 1g
10-20 days $712.31
1-Cyclopentyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea
This compound is primarily utilized in organic synthesis and medicinal chemistry as a key intermediate in the development of boron-containing molecules. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and organic materials. Additionally, its urea moiety can contribute to hydrogen bonding interactions, making it useful in the design of enzyme inhibitors or receptor ligands. The compound is often explored in drug discovery for its potential to enhance binding affinity and selectivity in target molecules. Its stability and reactivity also make it suitable for use in bioconjugation and labeling applications in chemical biology.
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