N-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)morpholine-4-carboxamide

98%

Reagent Code: #90453
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CAS Number 874290-97-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 332.2 g/mol
Formula C₁₇H₂₅BN₂O₄
badge Registry Numbers
MDL Number MFCD08689495
thermostat Physical Properties
Melting Point 248-250°C
Boiling Point 518.8°C
inventory_2 Storage & Handling
Density 1.16g/mL
Storage  2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester group makes it a valuable intermediate for constructing complex molecules, especially in pharmaceutical research and development. It is often employed in the synthesis of biologically active compounds, including potential drug candidates, due to its ability to facilitate the formation of carbon-carbon bonds. Additionally, it serves as a building block in the preparation of advanced materials, such as polymers and organic electronic components, where precise molecular architecture is required. Its morpholine moiety further enhances its utility in medicinal chemistry by contributing to the solubility and bioavailability of the target molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days £70.62
inventory 1g
10-20 days £191.98
N-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)morpholine-4-carboxamide
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester group makes it a valuable intermediate for constructing complex molecules, especially in pharmaceutical research and development. It is often employed in the synthesis of biologically active compounds, including potential drug candidates, due to its ability to facilitate the formation of carbon-carbon bonds. Additionally, it serves as a building block in the preparation of advanced materials, such as polymers and organic electronic components, where precise molecular architecture is required. Its morpholine moiety further enhances its utility in medicinal chemistry by contributing to the solubility and bioavailability of the target molecules.
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