Ethyl 5-bromo-4-methylbenzofuran-2-carboxylate

98%

Reagent Code: #182533
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CAS Number 1192172-68-1

science Other reagents with same CAS 1192172-68-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 283.12 g/mol
Formula C₁₂H₁₁BrO₃
thermostat Physical Properties
Boiling Point 393.8°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and anticancer compounds. Its structure allows for further functionalization, making it valuable in medicinal chemistry for building complex benzofuran-based molecules. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds, enabling the construction of diverse organic frameworks. Also utilized in research settings for designing novel bioactive molecules and in the preparation of fluorescent dyes due to the inherent optical properties of the benzofuran core.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿660.00
inventory 100mg
10-20 days ฿1,240.00

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Ethyl 5-bromo-4-methylbenzofuran-2-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and anticancer compounds. Its structure allows for further functionalization, making it valuable in medicinal chemistry for building complex benzofuran-based molecules. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds, enabling the construction of diverse organic frameworks. Also utilized in research settings for designing nov

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and anticancer compounds. Its structure allows for further functionalization, making it valuable in medicinal chemistry for building complex benzofuran-based molecules. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds, enabling the construction of diverse organic frameworks. Also utilized in research settings for designing novel bioactive molecules and in the preparation of fluorescent dyes due to the inherent optical properties of the benzofuran core.

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