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

95%

Reagent Code: #79944
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CAS Number 874298-10-9

science Other reagents with same CAS 874298-10-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 346.27204 g/mol
Formula C₁₉H₃₁BN₂O₃
badge Registry Numbers
MDL Number MFCD22494493
inventory_2 Storage & Handling
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description Product Description

This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. Its structure, featuring a urea moiety and a boronic ester group, makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions. These reactions are crucial for forming carbon-carbon bonds, enabling the synthesis of complex molecules used in drug discovery and development. Additionally, the boronic ester group can serve as a protective group for boron-containing compounds, which are often employed in targeted drug delivery systems. Its application extends to the preparation of bioactive molecules, including potential anticancer and anti-inflammatory agents, due to its ability to interact with specific biological targets.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿18,900.00
inventory 50mg
10-20 days ฿4,842.00

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1,1-Dipropyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea
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This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. Its structure, featuring a urea moiety and a boronic ester group, makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions. These reactions are crucial for forming carbon-carbon bonds, enabling the synthesis of complex molecules used in drug discovery and development. Additionally, the boronic ester group can serve as a protective group for boron-containin

This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. Its structure, featuring a urea moiety and a boronic ester group, makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions. These reactions are crucial for forming carbon-carbon bonds, enabling the synthesis of complex molecules used in drug discovery and development. Additionally, the boronic ester group can serve as a protective group for boron-containing compounds, which are often employed in targeted drug delivery systems. Its application extends to the preparation of bioactive molecules, including potential anticancer and anti-inflammatory agents, due to its ability to interact with specific biological targets.

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