Ethyl 1H-indole-4-carboxylate

98%

Reagent Code: #182491
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CAS Number 50614-84-1

science Other reagents with same CAS 50614-84-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.21 g/mol
Formula C₁₁H₁₁NO₂
thermostat Physical Properties
Boiling Point 342.4°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in pharmaceutical synthesis as an intermediate for developing bioactive molecules, particularly in the production of serotonin receptor modulators and anti-inflammatory agents. Commonly employed in research settings to construct indole-based compounds with potential neurological and anticancer activity. Also utilized in the development of fluorescent dyes and sensors due to the indole core’s favorable photophysical properties. Its ester functionality allows for easy modification in multi-step organic syntheses.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,290.00
inventory 250mg
10-20 days ฿510.00

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Ethyl 1H-indole-4-carboxylate
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Used in pharmaceutical synthesis as an intermediate for developing bioactive molecules, particularly in the production of serotonin receptor modulators and anti-inflammatory agents. Commonly employed in research settings to construct indole-based compounds with potential neurological and anticancer activity. Also utilized in the development of fluorescent dyes and sensors due to the indole core’s favorable photophysical properties. Its ester functionality allows for easy modification in multi-step organi

Used in pharmaceutical synthesis as an intermediate for developing bioactive molecules, particularly in the production of serotonin receptor modulators and anti-inflammatory agents. Commonly employed in research settings to construct indole-based compounds with potential neurological and anticancer activity. Also utilized in the development of fluorescent dyes and sensors due to the indole core’s favorable photophysical properties. Its ester functionality allows for easy modification in multi-step organic syntheses.

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