7-Methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
98%
Reagent
Code: #192707
CAS Number
912331-68-1
science Other reagents with same CAS 912331-68-1
blur_circular Chemical Specifications
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Molecular Information
Weight
257.14 g/mol
Formula
C₁₅H₂₀BNO₂
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Registry Numbers
MDL Number
MFCD11858374
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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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