Methyl 2-methyl-1H-indole-3-carboxylate

98%

Reagent Code: #206688
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CAS Number 65417-22-3

science Other reagents with same CAS 65417-22-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.21 g/mol
Formula C₁₁H₁₁NO₂
thermostat Physical Properties
Melting Point 165°C
Boiling Point 331.7±22.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in pharmaceutical research as an intermediate in the synthesis of bioactive compounds, particularly those targeting neurological and psychiatric disorders. Its indole core structure supports activity in serotonin and melatonin receptor pathways, making it valuable in developing central nervous system agents. Also employed in the preparation of fluorescent dyes and optical materials due to its favorable photophysical properties. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies of indole-based drug candidates.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿234.00
inventory 1g
10-20 days ฿670.00

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Methyl 2-methyl-1H-indole-3-carboxylate
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Used in pharmaceutical research as an intermediate in the synthesis of bioactive compounds, particularly those targeting neurological and psychiatric disorders. Its indole core structure supports activity in serotonin and melatonin receptor pathways, making it valuable in developing central nervous system agents. Also employed in the preparation of fluorescent dyes and optical materials due to its favorable photophysical properties. Commonly utilized in medicinal chemistry for structure-activity relation

Used in pharmaceutical research as an intermediate in the synthesis of bioactive compounds, particularly those targeting neurological and psychiatric disorders. Its indole core structure supports activity in serotonin and melatonin receptor pathways, making it valuable in developing central nervous system agents. Also employed in the preparation of fluorescent dyes and optical materials due to its favorable photophysical properties. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies of indole-based drug candidates.

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