(2-Oxoindolin-6-yl)boronic acid
97%
Reagent
Code: #116202
CAS Number
1217500-61-2
blur_circular Chemical Specifications
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Molecular Information
Weight
176.97 g/mol
Formula
C₈H₈BNO₃
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Registry Numbers
MDL Number
MFCD12913936
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Storage & Handling
Storage
2-8°C, store under inert gas
description Product Description
Used in organic synthesis as a key intermediate for the preparation of various pharmaceutical compounds, particularly in the development of kinase inhibitors. It is also employed in Suzuki-Miyaura cross-coupling reactions to create complex molecules for drug discovery and material science. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in constructing bioactive molecules and functional materials. Additionally, it plays a role in the development of targeted cancer therapies and other medicinal agents.
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