5-Bromo-3-methyl-1H-indole-2-carboxylic acid

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Reagent Code: #148495
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CAS Number 70070-32-5

science Other reagents with same CAS 70070-32-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.08 g/mol
Formula C₁₀H₈BrNO₂
badge Registry Numbers
MDL Number MFCD01366202
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of serotonin receptor modulators and other central nervous system agents. Its structure supports the construction of complex indole-based molecules with biological activity. Commonly employed in research settings for the preparation of analogs in medicinal chemistry programs targeting neurological disorders and inflammation. Also utilized in the creation of fluorescent probes due to the indole core’s photophysical properties, enabling applications in bioimaging and molecular sensing.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿560.00
inventory 250mg
10-20 days ฿1,340.00
inventory 1g
10-20 days ฿4,830.00

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5-Bromo-3-methyl-1H-indole-2-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of serotonin receptor modulators and other central nervous system agents. Its structure supports the construction of complex indole-based molecules with biological activity. Commonly employed in research settings for the preparation of analogs in medicinal chemistry programs targeting neurological disorders and inflammation. Also utilized in the creation of fluorescent probes due to the indole core’s pho
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of serotonin receptor modulators and other central nervous system agents. Its structure supports the construction of complex indole-based molecules with biological activity. Commonly employed in research settings for the preparation of analogs in medicinal chemistry programs targeting neurological disorders and inflammation. Also utilized in the creation of fluorescent probes due to the indole core’s photophysical properties, enabling applications in bioimaging and molecular sensing.
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