Methyl 5-bromo-1H-indole-3-carboxylate

98%

Reagent Code: #211025
label
Alias 5-Bromoindole-3-carboxylic acid methyl ester
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CAS Number 773873-77-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.08 g/mol
Formula C₁₀H₈BrNO₂
badge Registry Numbers
MDL Number MFCD06203728
thermostat Physical Properties
Boiling Point 386.2 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals and bioactive compounds, particularly in the development of serotonin receptor modulators and other neuroactive agents. Its structure supports the construction of complex indole-based molecules, making it valuable in medicinal chemistry research. Commonly employed in the preparation of tryptamine and tryptophan derivatives, it plays a role in studies related to central nervous system disorders. Also utilized in the creation of fluorescent probes and labeled compounds for biochemical assays due to the reactivity of the bromine moiety, which allows for further functionalization via cross-coupling reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿500.00
inventory 5g
10-20 days ฿2,470.00
inventory 25g
10-20 days ฿11,190.00
Methyl 5-bromo-1H-indole-3-carboxylate
Used primarily as a key intermediate in the synthesis of pharmaceuticals and bioactive compounds, particularly in the development of serotonin receptor modulators and other neuroactive agents. Its structure supports the construction of complex indole-based molecules, making it valuable in medicinal chemistry research. Commonly employed in the preparation of tryptamine and tryptophan derivatives, it plays a role in studies related to central nervous system disorders. Also utilized in the creation of fluorescent probes and labeled compounds for biochemical assays due to the reactivity of the bromine moiety, which allows for further functionalization via cross-coupling reactions.
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