2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-imidazole

98%

Reagent Code: #115706
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CAS Number 1229584-17-1

science Other reagents with same CAS 1229584-17-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 270.13 g/mol
Formula C₁₅H₁₉BN₂O₂
badge Registry Numbers
MDL Number MFCD18383629
inventory_2 Storage & Handling
Storage 2-8°C, inert gas

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a key intermediate for constructing complex organic molecules. Its boronate ester group (4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl) enables efficient coupling with aryl or vinyl halides, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. As an imidazole derivative, it is especially applied in the synthesis of larger imidazole-containing compounds, which are explored for their biological activity in drug discovery and development. Its stability and reactivity make it a versatile tool in medicinal chemistry and materials science research.

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inventory 100mg
10-20 days ฿9,450.00

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2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-imidazole
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a key intermediate for constructing complex organic molecules. Its boronate ester group (4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl) enables efficient coupling with aryl or vinyl halides, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. As an imidazole derivative, it is especially applied in the synthesis

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a key intermediate for constructing complex organic molecules. Its boronate ester group (4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl) enables efficient coupling with aryl or vinyl halides, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. As an imidazole derivative, it is especially applied in the synthesis of larger imidazole-containing compounds, which are explored for their biological activity in drug discovery and development. Its stability and reactivity make it a versatile tool in medicinal chemistry and materials science research.

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