(1H-Indol-2-yl)boronic acid
≥95%
Reagent
Code: #191352
CAS Number
220396-46-3
science Other reagents with same CAS 220396-46-3
blur_circular Chemical Specifications
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Molecular Information
Weight
160.967 g/mol
Formula
C₈H₈BNO₂
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Registry Numbers
MDL Number
MFCD08234622
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Storage & Handling
Storage
-20°C, Inert Gas
description Product Description
Used in organic synthesis as a building block for pharmaceuticals and biologically active compounds. Its boronic acid group enables Suzuki-Miyaura cross-coupling reactions, allowing the formation of carbon-carbon bonds in the development of complex indole derivatives. Commonly applied in medicinal chemistry for constructing drug candidates targeting cancer, inflammation, and neurological disorders. Also employed in the synthesis of fluorescent probes and functional materials due to the indole core’s electronic properties.
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