4-Chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole

98%

Reagent Code: #192493
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CAS Number 1256358-95-8

science Other reagents with same CAS 1256358-95-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 277.55 g/mol
Formula C₁₄H₁₇BClNO₂
badge Registry Numbers
MDL Number MFCD11858364
thermostat Physical Properties
Boiling Point 424.9±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.20±0.1 g/cm3(Predicted)
Storage -20°C, Sealed, Inert Gas

description Product Description

Used primarily as a key intermediate in pharmaceutical synthesis, especially in Suzuki-Miyaura cross-coupling reactions to construct biaryl frameworks found in bioactive molecules. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of indole-based drug candidates. Commonly applied in research settings for the synthesis of serotonin receptor modulators, anti-inflammatory agents, and kinase inhibitors. Also utilized in the preparation of functional materials and fluorescent probes due to the indole core’s inherent photophysical properties.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿13,300.00
inventory 250mg
10-20 days ฿4,920.00

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4-Chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
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Used primarily as a key intermediate in pharmaceutical synthesis, especially in Suzuki-Miyaura cross-coupling reactions to construct biaryl frameworks found in bioactive molecules. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of indole-based drug candidates. Commonly applied in research settings for the synthesis of serotonin receptor modulators, anti-inflammatory agents, and kinase inhibitors. Also utilized in the preparation of functional materials and fluorescent probes due to the indole core’s inherent photophysical properties.
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