Methyl 5-fluoro-3-formyl-1H-indole-2-carboxylate

95%

Reagent Code: #48548
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CAS Number 843629-51-6

science Other reagents with same CAS 843629-51-6

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scatter_plot Molecular Information
Weight 221.1845 g/mol
Formula C₁₁H₈FNO₃
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description Product Description

This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of indole-based drugs, which are known for their diverse biological activities. The presence of a formyl group at the 3-position, a methyl carboxylate at the 2-position, and a fluoro substituent at the 5-position makes it a versatile building block for creating molecules with potential anticancer, anti-inflammatory, or antimicrobial properties. Additionally, it is often employed in medicinal chemistry to explore structure-activity relationships (SAR) for optimizing drug candidates. Its role in the synthesis of heterocyclic compounds also extends to agrochemical research, where it contributes to the development of novel pesticides or herbicides.

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Test Parameter Specification
Appearance Yellow Solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,230.00

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Methyl 5-fluoro-3-formyl-1H-indole-2-carboxylate
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This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of indole-based drugs, which are known for their diverse biological activities. The presence of a formyl group at the 3-position, a methyl carboxylate at the 2-position, and a fluoro substituent at the 5-position makes it a versatile building block for creating molecules with potential anticancer, anti-inflammatory, or antimicrobial

This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of indole-based drugs, which are known for their diverse biological activities. The presence of a formyl group at the 3-position, a methyl carboxylate at the 2-position, and a fluoro substituent at the 5-position makes it a versatile building block for creating molecules with potential anticancer, anti-inflammatory, or antimicrobial properties. Additionally, it is often employed in medicinal chemistry to explore structure-activity relationships (SAR) for optimizing drug candidates. Its role in the synthesis of heterocyclic compounds also extends to agrochemical research, where it contributes to the development of novel pesticides or herbicides.

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