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

98%

Reagent Code: #192707
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CAS Number 912331-68-1

science Other reagents with same CAS 912331-68-1

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Weight 257.14 g/mol
Formula C₁₅H₂₀BNO₂
badge Registry Numbers
MDL Number MFCD11858374
inventory_2 Storage & Handling
Storage -20°C, Sealed, Inert Gas

description Product Description

Used primarily as a key intermediate in pharmaceutical synthesis, this compound plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. Its indole scaffold is commonly found in bioactive compounds, making it valuable in the development of drug candidates targeting neurological disorders, inflammation, and cancer. The boronate ester group allows for efficient and selective coupling with aryl halides under mild conditions, enhancing its utility in medicinal chemistry and late-stage functionalization of drug molecules. It is also employed in the synthesis of advanced intermediates for agrochemicals and functional materials.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,550.00
inventory 1g
10-20 days ฿9,610.00

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7-Methyl-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 synthesis, this compound plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. Its indole scaffold is commonly found in bioactive compounds, making it valuable in the development of drug candidates targeting neurological disorders, inflammation, and cancer. The boronate ester group allows for efficient and selective coupling with aryl halides under mild conditions, enhancing its utility in medicinal chemistry and late-stage functionalization of drug molecules. It is also employed in the synthesis of advanced intermediates for agrochemicals and functional materials.
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