Ethyl 2-(1H-indol-3-yl)-2-oxoacetate

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Reagent Code: #185290
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CAS Number 51079-10-8

science Other reagents with same CAS 51079-10-8

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scatter_plot Molecular Information
Weight 217.226 g/mol
Formula C₁₂H₁₁NO₃
badge Registry Numbers
MDL Number MFCD00085450
inventory_2 Storage & Handling
Storage 2-8°C, drying away from light

description Product Description

Used as a key intermediate in the synthesis of indole-based pharmaceuticals, particularly in the preparation of tryptophan derivatives and bioactive molecules with potential antitumor, antiviral, and anti-inflammatory properties. Its structure allows for easy functionalization at the indole ring and ester group, making it valuable in medicinal chemistry for building complex heterocyclic compounds. Commonly employed in research settings to develop new drug candidates targeting neurological disorders and cancer. Also utilized in the preparation of fluorescent probes due to the inherent optical properties of the indole scaffold.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿7,250.00
inventory 10g
10-20 days ฿14,490.00
inventory 25g
10-20 days ฿31,470.00
inventory 1g
10-20 days ฿1,460.00

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Ethyl 2-(1H-indol-3-yl)-2-oxoacetate
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Used as a key intermediate in the synthesis of indole-based pharmaceuticals, particularly in the preparation of tryptophan derivatives and bioactive molecules with potential antitumor, antiviral, and anti-inflammatory properties. Its structure allows for easy functionalization at the indole ring and ester group, making it valuable in medicinal chemistry for building complex heterocyclic compounds. Commonly employed in research settings to develop new drug candidates targeting neurological disorders and c

Used as a key intermediate in the synthesis of indole-based pharmaceuticals, particularly in the preparation of tryptophan derivatives and bioactive molecules with potential antitumor, antiviral, and anti-inflammatory properties. Its structure allows for easy functionalization at the indole ring and ester group, making it valuable in medicinal chemistry for building complex heterocyclic compounds. Commonly employed in research settings to develop new drug candidates targeting neurological disorders and cancer. Also utilized in the preparation of fluorescent probes due to the inherent optical properties of the indole scaffold.

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