(1-(tert-Butoxycarbonyl)-1H-indol-4-yl)boronic acid

95%

Reagent Code: #148563
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CAS Number 2102451-30-7

science Other reagents with same CAS 2102451-30-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 261.08 g/mol
Formula C₁₃H₁₆BNO₄
badge Registry Numbers
MDL Number MFCD28130132
inventory_2 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.

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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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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,006.50
inventory 250mg
10-20 days ฿1,622.50
inventory 1g
10-20 days ฿4,543.00

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(1-(tert-Butoxycarbonyl)-1H-indol-4-yl)boronic acid
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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 medicina
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.
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