Methyl 4-bromo-1H-indole-2-carboxylate

98%

Reagent Code: #207572
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CAS Number 167479-13-2

science Other reagents with same CAS 167479-13-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.08 g/mol
Formula C₁₀H₈BrNO₂
badge Registry Numbers
MDL Number MFCD04966956
thermostat Physical Properties
Boiling Point 386.2°C
inventory_2 Storage & Handling
Density 1.629 g/mL
Storage Room temperature, dry

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds, particularly in the development of indole-based drugs. Commonly employed in the preparation of serotonin receptor ligands and kinase inhibitors. Also serves as a building block in the synthesis of tryptophan derivatives and other nitrogen-containing heterocycles. Frequently utilized in medicinal chemistry research for structure-activity relationship (SAR) studies due to its substituted indole core.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿742.50
inventory 5g
10-20 days ฿6,570.00
inventory 25g
10-20 days ฿31,960.00

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Methyl 4-bromo-1H-indole-2-carboxylate
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds, particularly in the development of indole-based drugs. Commonly employed in the preparation of serotonin receptor ligands and kinase inhibitors. Also serves as a building block in the synthesis of tryptophan derivatives and other nitrogen-containing heterocycles. Frequently utilized in medicinal chemistry research for structure-activity relationship (SAR) studies due to its substituted indole core.

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds, particularly in the development of indole-based drugs. Commonly employed in the preparation of serotonin receptor ligands and kinase inhibitors. Also serves as a building block in the synthesis of tryptophan derivatives and other nitrogen-containing heterocycles. Frequently utilized in medicinal chemistry research for structure-activity relationship (SAR) studies due to its substituted indole core.

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