4-Methoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole

95%

Reagent Code: #192683
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CAS Number 1072811-21-2

science Other reagents with same CAS 1072811-21-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 273.14 g/mol
Formula C₁₅H₂₀BNO₃
badge Registry Numbers
MDL Number MFCD11858387
inventory_2 Storage & Handling
Storage -20°C, Sealed, Inert Gas

description Product Description

Used primarily as a key intermediate in pharmaceutical and agrochemical synthesis, this compound enables the formation of carbon-carbon bonds through Suzuki-Miyaura cross-coupling reactions. Its boronate ester group facilitates mild and selective coupling with aryl or heteroaryl halides, making it valuable in constructing complex indole derivatives. These derivatives are commonly found in bioactive molecules, including drug candidates targeting inflammation, cancer, and neurological disorders. The methoxy group enhances electronic properties and stability, improving reaction efficiency and selectivity. It is also employed in materials science for developing organic semiconductors and fluorescent probes due to the indole core’s favorable photophysical characteristics.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,930.00
inventory 1g
10-20 days ฿13,300.00

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4-Methoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
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Used primarily as a key intermediate in pharmaceutical and agrochemical synthesis, this compound enables the formation of carbon-carbon bonds through Suzuki-Miyaura cross-coupling reactions. Its boronate ester group facilitates mild and selective coupling with aryl or heteroaryl halides, making it valuable in constructing complex indole derivatives. These derivatives are commonly found in bioactive molecules, including drug candidates targeting inflammation, cancer, and neurological disorders. The methoxy group enhances electronic properties and stability, improving reaction efficiency and selectivity. It is also employed in materials science for developing organic semiconductors and fluorescent probes due to the indole core’s favorable photophysical characteristics.
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