Methyl 7-bromo-1H-indole-5-carboxylate

96%

Reagent Code: #207340
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CAS Number 885523-35-3

science Other reagents with same CAS 885523-35-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.08 g/mol
Formula C₁₀H₈BrNO₂
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds, particularly in the development of serotonin receptor modulators and other central nervous system agents. Its bromo and ester functional groups allow for further chemical modifications, making it valuable in constructing complex indole-based structures. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds. Also utilized in medicinal chemistry research for generating libraries of indole derivatives with potential anti-inflammatory, antiviral, or anticancer activities.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿640.00
inventory 100mg
10-20 days ฿1,250.00
inventory 250mg
10-20 days ฿2,350.00
inventory 1g
10-20 days ฿8,120.00
inventory 5g
10-20 days ฿31,820.00

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Methyl 7-bromo-1H-indole-5-carboxylate
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds, particularly in the development of serotonin receptor modulators and other central nervous system agents. Its bromo and ester functional groups allow for further chemical modifications, making it valuable in constructing complex indole-based structures. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds. Also utilized in medicinal chemistry research for generat

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds, particularly in the development of serotonin receptor modulators and other central nervous system agents. Its bromo and ester functional groups allow for further chemical modifications, making it valuable in constructing complex indole-based structures. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds. Also utilized in medicinal chemistry research for generating libraries of indole derivatives with potential anti-inflammatory, antiviral, or anticancer activities.

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