(2-Oxoindolin-5-yl)boronic acid
≥98%
Reagent
Code: #222359
CAS Number
1051316-38-1
science Other reagents with same CAS 1051316-38-1
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
MFCD10696667
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Storage & Handling
Storage
-20°C, Sealed, Drying, Inert Gas
description Product Description
Used in organic synthesis as a key intermediate for pharmaceuticals, particularly in the preparation of kinase inhibitors and anti-cancer agents. Its boronic acid functionality enables Suzuki-Miyaura cross-coupling reactions, allowing the formation of carbon-carbon bonds in complex molecule assembly. Commonly employed in medicinal chemistry for constructing indole-based scaffolds, which are prevalent in bioactive molecules. Also utilized in the development of protease inhibitors and targeted therapies due to its structural compatibility with biological systems.
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