Ethyl 1-methyl-1H-indole-2-carboxylate

98%

Reagent Code: #180629
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CAS Number 18450-24-3

science Other reagents with same CAS 18450-24-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.24 g/mol
Formula C₁₂H₁₃NO₂
badge Registry Numbers
MDL Number MFCD01926673
thermostat Physical Properties
Melting Point 59-60 °C
Boiling Point 333.5±15.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.11±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor modulators and other central nervous system agents. Commonly employed in research settings to construct indole-based scaffolds, which are prevalent in bioactive molecules and drug candidates. Also utilized in the preparation of analogs for structure-activity relationship (SAR) studies due to the ease of functionalization at the indole core. Its ester group allows for straightforward conversion to amides or acids, enabling further derivatization in medicinal chemistry workflows.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,530.00
inventory 250mg
10-20 days ฿9,410.00
inventory 1g
10-20 days ฿25,380.00

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Ethyl 1-methyl-1H-indole-2-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor modulators and other central nervous system agents. Commonly employed in research settings to construct indole-based scaffolds, which are prevalent in bioactive molecules and drug candidates. Also utilized in the preparation of analogs for structure-activity relationship (SAR) studies due to the ease of functionalization at the indole core. Its ester group allows for straightforward conve

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor modulators and other central nervous system agents. Commonly employed in research settings to construct indole-based scaffolds, which are prevalent in bioactive molecules and drug candidates. Also utilized in the preparation of analogs for structure-activity relationship (SAR) studies due to the ease of functionalization at the indole core. Its ester group allows for straightforward conversion to amides or acids, enabling further derivatization in medicinal chemistry workflows.

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