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

97%

Reagent Code: #210468
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CAS Number 851524-90-8

science Other reagents with same CAS 851524-90-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.14 g/mol
Formula C₁₅H₂₀BNO₂
badge Registry Numbers
MDL Number MFCD16995803
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. It enables the formation of carbon-carbon bonds, particularly in the construction of biaryl or heteroaryl frameworks found in pharmaceuticals and agrochemicals. The indole core makes it valuable for synthesizing bioactive molecules, including drug candidates targeting neurological disorders, inflammation, and cancer. Its boronate ester group offers stability and reactivity under mild conditions, making it suitable for late-stage functionalization in complex molecule assembly. Commonly employed in medicinal chemistry and materials science for building advanced intermediates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,680.00
inventory 250mg
10-20 days ฿9,280.00
inventory 1g
10-20 days ฿22,040.00

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3-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
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Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. It enables the formation of carbon-carbon bonds, particularly in the construction of biaryl or heteroaryl frameworks found in pharmaceuticals and agrochemicals. The indole core makes it valuable for synthesizing bioactive molecules, including drug candidates targeting neurological disorders, inflammation, and cancer. Its boronate ester group offers stability and reactivity under mild condit

Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. It enables the formation of carbon-carbon bonds, particularly in the construction of biaryl or heteroaryl frameworks found in pharmaceuticals and agrochemicals. The indole core makes it valuable for synthesizing bioactive molecules, including drug candidates targeting neurological disorders, inflammation, and cancer. Its boronate ester group offers stability and reactivity under mild conditions, making it suitable for late-stage functionalization in complex molecule assembly. Commonly employed in medicinal chemistry and materials science for building advanced intermediates.

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