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

≥98%

Reagent Code: #203098
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CAS Number 837392-54-8

science Other reagents with same CAS 837392-54-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.13 g/mol
Formula C₁₅H₂₀BNO₂
badge Registry Numbers
MDL Number MFCD13181964
thermostat Physical Properties
Boiling Point 407.8±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.09±0.1 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used in organic synthesis as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its indole core makes it valuable for constructing bioactive molecules, particularly in the synthesis of tryptamine or tryptophan derivatives. Commonly employed in medicinal chemistry for building complex heterocyclic structures with potential activity in central nervous system drugs and anticancer agents. Also utilized in materials science for creating organic semiconductors and fluorescent dyes due to the indole’s electron-rich nature.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,030.00
inventory 250mg
10-20 days ฿5,140.00
inventory 1g
10-20 days ฿13,350.00
2-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
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Used in organic synthesis as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its indole core makes it valuable for constructing bioactive molecules, particularly in the synthesis of tryptamine or tryptophan derivatives. Commonly employed in medicinal chemistry for building complex heterocyclic structures with potential activity in central nervous system drugs and anticancer agents. Also utilized i

Used in organic synthesis as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its indole core makes it valuable for constructing bioactive molecules, particularly in the synthesis of tryptamine or tryptophan derivatives. Commonly employed in medicinal chemistry for building complex heterocyclic structures with potential activity in central nervous system drugs and anticancer agents. Also utilized in materials science for creating organic semiconductors and fluorescent dyes due to the indole’s electron-rich nature.

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