Ethyl 6-nitro-1H-indole-2-carboxylate

≥97%

Reagent Code: #184891
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CAS Number 16792-45-3

science Other reagents with same CAS 16792-45-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.21 g/mol
Formula C₁₁H₁₀N₂O₄
badge Registry Numbers
MDL Number MFCD04973967
thermostat Physical Properties
Boiling Point 429.5 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of indole-based drugs with potential anti-inflammatory, antiviral, and anticancer activities. Its nitro group allows for further chemical modifications, making it valuable in medicinal chemistry for building complex heterocyclic systems. Also employed in research settings to design new bioactive molecules and in the preparation of fluorescent dyes and sensors due to the inherent optical properties of the indole scaffold.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,780.00
inventory 250mg
10-20 days ฿2,990.00
inventory 5g
10-20 days ฿35,450.00
inventory 1g
10-20 days ฿9,560.00

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Ethyl 6-nitro-1H-indole-2-carboxylate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of indole-based drugs with potential anti-inflammatory, antiviral, and anticancer activities. Its nitro group allows for further chemical modifications, making it valuable in medicinal chemistry for building complex heterocyclic systems. Also employed in research settings to design new bioactive molecules and in the preparation of fluorescent dyes and sensors due to the inherent optical properties of the indole s

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of indole-based drugs with potential anti-inflammatory, antiviral, and anticancer activities. Its nitro group allows for further chemical modifications, making it valuable in medicinal chemistry for building complex heterocyclic systems. Also employed in research settings to design new bioactive molecules and in the preparation of fluorescent dyes and sensors due to the inherent optical properties of the indole scaffold.

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