tert-Butyl 3-bromo-1H-indole-1-carboxylate

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Reagent Code: #145554
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CAS Number 143259-56-7

science Other reagents with same CAS 143259-56-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.16 g/mol
Formula C₁₃H₁₄BrNO₂
thermostat Physical Properties
Boiling Point 367.8°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the production of indole-based bioactive compounds. It serves as a protected indole derivative, allowing selective functionalization at other positions of the indole ring during multi-step reactions. Commonly employed in the development of serotonin receptor modulators, kinase inhibitors, and anti-inflammatory agents. Its tert-butoxycarbonyl (Boc) group stabilizes the nitrogen, enabling cleaner reactions and easier purification in drug discovery processes. Also utilized in agrochemical research for designing novel active ingredients.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿144.00
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿1,280.00

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tert-Butyl 3-bromo-1H-indole-1-carboxylate
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Used as an intermediate in pharmaceutical synthesis, particularly in the production of indole-based bioactive compounds. It serves as a protected indole derivative, allowing selective functionalization at other positions of the indole ring during multi-step reactions. Commonly employed in the development of serotonin receptor modulators, kinase inhibitors, and anti-inflammatory agents. Its tert-butoxycarbonyl (Boc) group stabilizes the nitrogen, enabling cleaner reactions and easier purification in drug

Used as an intermediate in pharmaceutical synthesis, particularly in the production of indole-based bioactive compounds. It serves as a protected indole derivative, allowing selective functionalization at other positions of the indole ring during multi-step reactions. Commonly employed in the development of serotonin receptor modulators, kinase inhibitors, and anti-inflammatory agents. Its tert-butoxycarbonyl (Boc) group stabilizes the nitrogen, enabling cleaner reactions and easier purification in drug discovery processes. Also utilized in agrochemical research for designing novel active ingredients.

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