Ethyl 7-bromo-1H-indole-2-carboxylate

95%

  • Product Code: 52040
  Alias:    Ethyl 7-bromo-2-indolecarboxylate;
  CAS:    16732-69-7
Molecular Weight: 268.11 g./mol Molecular Formula: C₁₁H₁₀BrNO₂
EC Number: MDL Number: MFCD04972046
Melting Point: Boiling Point: 394.7ºC
Density: 1.554 g/cm3 Storage Condition: Room temperature, dry, sealed
Product Description: Ethyl 7-bromo-1H-indole-2-carboxylate is primarily used in organic synthesis as a key intermediate for the development of more complex indole derivatives. Its bromo and ester functional groups make it a versatile building block in pharmaceutical research, particularly for the synthesis of compounds with potential biological activity. It is often employed in the construction of indole-based molecules that are explored for their therapeutic properties, such as anti-inflammatory, anticancer, or antimicrobial agents. Additionally, this compound is utilized in the study of structure-activity relationships (SAR) to optimize the efficacy and selectivity of drug candidates. Its reactivity also allows for further functionalization, enabling the creation of diverse chemical libraries for drug discovery programs.
Product Specification:
Test Specification
Purity 94.5 100%
Appearance WHITE TO LIGHT YELLOW SOLID
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿1,380.00
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5.000 10-20 days ฿4,700.00
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25.000 10-20 days ฿16,670.00
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Ethyl 7-bromo-1H-indole-2-carboxylate
Ethyl 7-bromo-1H-indole-2-carboxylate is primarily used in organic synthesis as a key intermediate for the development of more complex indole derivatives. Its bromo and ester functional groups make it a versatile building block in pharmaceutical research, particularly for the synthesis of compounds with potential biological activity. It is often employed in the construction of indole-based molecules that are explored for their therapeutic properties, such as anti-inflammatory, anticancer, or antimicrobial agents. Additionally, this compound is utilized in the study of structure-activity relationships (SAR) to optimize the efficacy and selectivity of drug candidates. Its reactivity also allows for further functionalization, enabling the creation of diverse chemical libraries for drug discovery programs.
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