(1-(tert-Butoxycarbonyl)-1H-indol-4-yl)boronic acid
95%
Reagent
Code: #148563
CAS Number
2102451-30-7
science Other reagents with same CAS 2102451-30-7
blur_circular Chemical Specifications
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Molecular Information
Weight
261.08 g/mol
Formula
C₁₃H₁₆BNO₄
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Registry Numbers
MDL Number
MFCD28130132
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Storage & Handling
Storage
2-8°C, stored in inert gas
description Product Description
Used as a key intermediate in pharmaceutical synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to construct biaryl compounds. Its indole boronic acid structure enables selective formation of carbon-carbon bonds, making it valuable in the development of drug candidates targeting kinase inhibitors and CNS-active agents. The Boc-protected indole ring enhances stability and solubility during reaction processes, allowing for efficient coupling under mild conditions. Commonly employed in medicinal chemistry for lead optimization in the discovery of bioactive molecules. Additionally, it serves as a starting material in the development of fluorescent compounds or organic materials for certain electronic devices.
format_list_bulleted Product Specification
| Test Parameter | Specification |
|---|---|
| Appearance | Light yellow to yellow powder or crystals |
| Purity (%) | 94.5-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
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