1-(2,2,2-Trifluoroethyl)-1h-indol-6-amine

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Reagent Code: #244335
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CAS Number 1178958-31-0

science Other reagents with same CAS 1178958-31-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.19 g/mol
Formula C₁₀H₉F₃N₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system (CNS) agents. It shows utility in creating analogs for serotonin and dopamine receptor modulators, making it valuable in research for antidepressants, antipsychotics, and cognitive enhancers. Its trifluoroethyl group enhances metabolic stability and blood-brain barrier penetration, which improves drug efficacy in neuroactive compounds. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid indole scaffold and electron-withdrawing substituent.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿8,900.00
100mg
10-20 days ฿22,260.00
500mg
10-20 days ฿69,630.00

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1-(2,2,2-Trifluoroethyl)-1h-indol-6-amine
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system (CNS) agents. It shows utility in creating analogs for serotonin and dopamine receptor modulators, making it valuable in research for antidepressants, antipsychotics, and cognitive enhancers. Its trifluoroethyl group enhances metabolic stability and blood-brain barrier penetration, which improves drug efficacy in neuroactive compounds. Also employed in medicinal chemistry for

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system (CNS) agents. It shows utility in creating analogs for serotonin and dopamine receptor modulators, making it valuable in research for antidepressants, antipsychotics, and cognitive enhancers. Its trifluoroethyl group enhances metabolic stability and blood-brain barrier penetration, which improves drug efficacy in neuroactive compounds. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid indole scaffold and electron-withdrawing substituent.

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