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

97%

Reagent Code: #184790
fingerprint
CAS Number 26304-51-8

science Other reagents with same CAS 26304-51-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.24 g/mol
Formula C₁₂H₁₃NO₂
badge Registry Numbers
MDL Number MFCD00225365
thermostat Physical Properties
Melting Point 134-138 °C
Boiling Point 195 °C/0.5mmHg(lit.)
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in pharmaceutical synthesis as an intermediate for bioactive compounds, particularly in the development of serotonin receptor modulators and other central nervous system agents. Commonly employed in the preparation of indole-based drug candidates due to its ability to mimic natural indole alkaloid structures. Also utilized in research settings for the synthesis of fluorescent dyes and optical materials owing to the inherent aromatic and electron-rich nature of the indole core. Its ester functionality allows for easy modification, making it a versatile building block in medicinal chemistry and heterocyclic compound development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,180.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Ethyl 3-methyl-1H-indole-2-carboxylate
No image available

Used in pharmaceutical synthesis as an intermediate for bioactive compounds, particularly in the development of serotonin receptor modulators and other central nervous system agents. Commonly employed in the preparation of indole-based drug candidates due to its ability to mimic natural indole alkaloid structures. Also utilized in research settings for the synthesis of fluorescent dyes and optical materials owing to the inherent aromatic and electron-rich nature of the indole core. Its ester functionalit

Used in pharmaceutical synthesis as an intermediate for bioactive compounds, particularly in the development of serotonin receptor modulators and other central nervous system agents. Commonly employed in the preparation of indole-based drug candidates due to its ability to mimic natural indole alkaloid structures. Also utilized in research settings for the synthesis of fluorescent dyes and optical materials owing to the inherent aromatic and electron-rich nature of the indole core. Its ester functionality allows for easy modification, making it a versatile building block in medicinal chemistry and heterocyclic compound development.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...