2-(5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-benzo[d]imidazol-1-yl)ethanol

98%

Reagent Code: #89641
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CAS Number 1491137-94-0

science Other reagents with same CAS 1491137-94-0

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scatter_plot Molecular Information
Weight 288.16 g/mol
Formula C₁₅H₂₁BN₂O₃
badge Registry Numbers
MDL Number MFCD28384367
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester group serves as a key functional moiety, enabling the formation of carbon-carbon bonds in the construction of complex organic molecules. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its benzimidazole moiety contributes to its potential use in the development of biologically active compounds, including drug candidates targeting various diseases. The compound’s stability and reactivity make it a versatile intermediate in medicinal chemistry and material science research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿19,380.00

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2-(5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-benzo[d]imidazol-1-yl)ethanol
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This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester group serves as a key functional moiety, enabling the formation of carbon-carbon bonds in the construction of complex organic molecules. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its benzimidazole moiety contributes to its potential use in the development of biologically active compound

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester group serves as a key functional moiety, enabling the formation of carbon-carbon bonds in the construction of complex organic molecules. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its benzimidazole moiety contributes to its potential use in the development of biologically active compounds, including drug candidates targeting various diseases. The compound’s stability and reactivity make it a versatile intermediate in medicinal chemistry and material science research.

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