4-(1H-Indol-2-yl)aniline

95%

Reagent Code: #192592
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CAS Number 21889-05-4

science Other reagents with same CAS 21889-05-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 208.26 g/mol
Formula C₁₄H₁₂N₂
badge Registry Numbers
MDL Number MFCD01719190
thermostat Physical Properties
Melting Point 201-202 °C(Solv: ethanol (64-17-5))
Boiling Point 441.2±20.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.229±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used primarily as a key intermediate in the synthesis of indole-based pharmaceuticals and bioactive compounds. It plays an important role in the development of serotonin receptor modulators and kinase inhibitors due to its structural similarity to endogenous indoleamines. Commonly employed in medicinal chemistry for constructing libraries of compounds targeting neurological disorders, inflammation, and cancer. Its aniline and indole functionalities allow for diverse functionalization, making it valuable in forming complex heterocyclic systems through coupling reactions and cyclizations. Also utilized in the preparation of fluorescent dyes and optical materials owing to its electron-rich aromatic framework.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,790.00
inventory 250mg
10-20 days ฿8,100.00
inventory 1g
10-20 days ฿21,970.00

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4-(1H-Indol-2-yl)aniline
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Used primarily as a key intermediate in the synthesis of indole-based pharmaceuticals and bioactive compounds. It plays an important role in the development of serotonin receptor modulators and kinase inhibitors due to its structural similarity to endogenous indoleamines. Commonly employed in medicinal chemistry for constructing libraries of compounds targeting neurological disorders, inflammation, and cancer. Its aniline and indole functionalities allow for diverse functionalization, making it valuable in forming complex heterocyclic systems through coupling reactions and cyclizations. Also utilized in the preparation of fluorescent dyes and optical materials owing to its electron-rich aromatic framework.
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