(1-tosyl-1H-Indol-3-yl)boronic acid

97%

Reagent Code: #196761
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CAS Number 149108-61-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 315.15 g/mol
Formula C₁₅H₁₄BNO₄S
badge Registry Numbers
MDL Number MFCD03093101
inventory_2 Storage & Handling
Storage -20°C, dry

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, particularly in the development of indole-based drug candidates. The tosyl group stabilizes the structure and can act as a protecting group, enabling selective reactions at other sites in the molecule. Commonly applied in the preparation of tryptamine and tryptophan analogs, as well as in the construction of complex heterocyclic systems found in natural products and medicinal agents.

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Test Parameter Specification
Appearance Solid
Purity (%) 96.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,370.00
inventory 250mg
10-20 days ฿4,530.00
inventory 1g
10-20 days ฿10,470.00
inventory 5g
10-20 days ฿42,150.00
(1-tosyl-1H-Indol-3-yl)boronic acid
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, particularly in the development of indole-based drug candidates. The tosyl group stabilizes the structure and can act as a protecting group, enabling selective reactions at other sites in the molecule. Commonly applied in the preparation of tryptamine and tryptophan analogs, as well as in the construction of complex heterocyclic systems found in natural products and medicinal agents.
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