Methyl 6-methyl-1H-indole-2-carboxylate

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Reagent Code: #211065
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CAS Number 18377-65-6

science Other reagents with same CAS 18377-65-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.21 g/mol
Formula C₁₁H₁₁NO₂
badge Registry Numbers
MDL Number MFCD06653197
thermostat Physical Properties
Melting Point 97-98 °C
Boiling Point 337.7±22.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.212±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor modulators and other central nervous system agents. Its indole core structure makes it valuable in creating analogs for drug discovery, especially in treatments targeting neurological disorders such as migraines, depression, and anxiety. Also employed in the preparation of bioactive molecules and agrochemicals due to its ability to participate in various coupling and functionalization reactions. Its ester group allows for easy modification, enabling the construction of complex molecular architectures in medicinal chemistry research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,330.00
inventory 250mg
10-20 days ฿2,750.00
inventory 1g
10-20 days ฿8,200.00

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Methyl 6-methyl-1H-indole-2-carboxylate
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Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor modulators and other central nervous system agents. Its indole core structure makes it valuable in creating analogs for drug discovery, especially in treatments targeting neurological disorders such as migraines, depression, and anxiety. Also employed in the preparation of bioactive molecules and agrochemicals due to its ability to participate in various coupling and functionalization reactions. Its ester group allows for easy modification, enabling the construction of complex molecular architectures in medicinal chemistry research.
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