1-(Phenylsulfonyl)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole

98%

Reagent Code: #227859
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CAS Number 1333344-24-3

science Other reagents with same CAS 1333344-24-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 383.27 g/mol
Formula C₂₀H₂₂BNO₄S
badge Registry Numbers
MDL Number MFCD12828207
thermostat Physical Properties
Boiling Point 556.4±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.21±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used in Suzuki-Miyaura cross-coupling reactions to synthesize complex indole derivatives, which are key scaffolds in pharmaceuticals and agrochemicals. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and development of bioactive molecules. Its sulfonyl group enhances stability and influences electronic properties, improving reaction selectivity. Commonly applied in the preparation of potential therapeutic agents, including kinase inhibitors and anti-inflammatory compounds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,430.00
inventory 1g
10-20 days ฿6,460.00
inventory 5g
10-20 days ฿19,800.00

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1-(Phenylsulfonyl)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
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Used in Suzuki-Miyaura cross-coupling reactions to synthesize complex indole derivatives, which are key scaffolds in pharmaceuticals and agrochemicals. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and development of bioactive molecules. Its sulfonyl group enhances stability and influences electronic properties, improving reaction selectivity. Commonly applied in the preparation of potential therapeutic agents, including kinase inhibitors and anti-inflammatory compounds.
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