5-Nitro-3-(trifluoromethyl)-1H-Indole

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Reagent Code: #215208
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CAS Number 1049026-43-8

science Other reagents with same CAS 1049026-43-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.1434 g/mol
Formula C₉H₅F₃N₂O₂
thermostat Physical Properties
Boiling Point 353.7±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.563±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential antitumor, antimicrobial, and anti-inflammatory properties. Its structure serves as a core scaffold in medicinal chemistry for designing inhibitors targeting specific enzymes and receptors. The electron-withdrawing nitro and trifluoromethyl groups enhance binding affinity and metabolic stability, making it valuable in optimizing drug candidates. Also employed in agrochemical research for developing novel pesticides and herbicides due to its ability to interact with biological targets in pests and weeds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿51,200.00

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5-Nitro-3-(trifluoromethyl)-1H-Indole
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Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential antitumor, antimicrobial, and anti-inflammatory properties. Its structure serves as a core scaffold in medicinal chemistry for designing inhibitors targeting specific enzymes and receptors. The electron-withdrawing nitro and trifluoromethyl groups enhance binding affinity and metabolic stability, making it valuable in optimizing drug candidates. Also employ

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential antitumor, antimicrobial, and anti-inflammatory properties. Its structure serves as a core scaffold in medicinal chemistry for designing inhibitors targeting specific enzymes and receptors. The electron-withdrawing nitro and trifluoromethyl groups enhance binding affinity and metabolic stability, making it valuable in optimizing drug candidates. Also employed in agrochemical research for developing novel pesticides and herbicides due to its ability to interact with biological targets in pests and weeds.

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