1-Phenyl-2-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1H-benzimidazole

≥98%

Reagent Code: #66400
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CAS Number 952514-86-2

science Other reagents with same CAS 952514-86-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 396.3 g/mol
Formula C₂₅H₂₅BN₂O₂
badge Registry Numbers
MDL Number MFCD16038225
thermostat Physical Properties
Melting Point 172-176°C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester functional group makes it a valuable intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. It is also employed in the synthesis of advanced materials, including organic semiconductors and light-emitting diodes (OLEDs), due to its ability to facilitate the formation of carbon-carbon bonds. Additionally, it serves as a key building block in the preparation of biologically active compounds, aiding in drug discovery and development processes.

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Test Parameter Specification
Appearance White to almost white powder to crystal
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿1,260.00
inventory 1g
10-20 days ฿4,800.00

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1-Phenyl-2-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1H-benzimidazole
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This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester functional group makes it a valuable intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. It is also employed in the synthesis of advanced materials, including organic semiconductors and light-emitting diodes (OLEDs), due to its ability to facilitate the formation of carbon-carbon bonds. Additionally, it serves as a key building block in the preparation of biologically active compounds, aiding in drug discovery and development processes.
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