2,2-Dimethyl-1-(4-methyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indol-1-yl)propan-1-one

98%

Reagent Code: #192908
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CAS Number 2390149-06-9

science Other reagents with same CAS 2390149-06-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 341.25 g/mol
Formula C₂₀H₂₈BNO₃
thermostat Physical Properties
Boiling Point 447.2±33.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.05±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used primarily in organic synthesis as a key intermediate in Suzuki-Miyaura cross-coupling reactions. Its boronate ester functionality allows for efficient carbon-carbon bond formation, making it valuable in the development of pharmaceuticals and agrochemicals. Commonly employed in the construction of complex indole derivatives, which are prevalent in bioactive molecules and drug candidates. The methyl and dimethyl groups enhance steric stability, improving selectivity during coupling. Suitable for research in medicinal chemistry and materials science where functionalized indoles are required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,270.00
inventory 250mg
10-20 days ฿3,860.00
inventory 1g
10-20 days ฿10,400.00

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2,2-Dimethyl-1-(4-methyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indol-1-yl)propan-1-one
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Used primarily in organic synthesis as a key intermediate in Suzuki-Miyaura cross-coupling reactions. Its boronate ester functionality allows for efficient carbon-carbon bond formation, making it valuable in the development of pharmaceuticals and agrochemicals. Commonly employed in the construction of complex indole derivatives, which are prevalent in bioactive molecules and drug candidates. The methyl and dimethyl groups enhance steric stability, improving selectivity during coupling. Suitable for research in medicinal chemistry and materials science where functionalized indoles are required.
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