(1-(Phenylsulfonyl)-1H-indol-3-yl)boronic acid
≥95%
Reagent
Code: #226227
CAS Number
129271-98-3
blur_circular Chemical Specifications
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Molecular Information
Weight
301.13 g/mol
Formula
C₁₄H₁₂BNO₄S
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Registry Numbers
MDL Number
MFCD02681892
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Physical Properties
Boiling Point
581.384°C at 760 mmHg
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Storage & Handling
Storage
2-8°C, protected from light, stored in inert gas
description Product Description
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active indole derivatives. Its boronic acid functionality allows for efficient carbon-carbon bond formation, making it valuable in pharmaceutical research and development of drug candidates targeting inflammation, cancer, and neurological disorders. The phenylsulfonyl group enhances stability and influences electronic properties, improving reaction selectivity and yield in heterocyclic compound synthesis. Commonly employed in medicinal chemistry for constructing complex indole-based scaffolds found in bioactive molecules.
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