2-(Trifluoromethyl)-1H-indole

98%

Reagent Code: #240693
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CAS Number 51310-54-4

science Other reagents with same CAS 51310-54-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 185.15 g/mol
Formula C₉H₆F₃N
badge Registry Numbers
MDL Number MFCD04972104
thermostat Physical Properties
Melting Point 106-110°C
Boiling Point 256.7°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antidepressants, antipsychotic drugs, antimicrobials, and anticancer agents. Its structure supports activity in central nervous system agents due to enhanced metabolic stability and binding affinity. The trifluoromethyl group improves cell permeability, lipophilicity, and bioavailability. Also employed in agrochemicals to improve the efficacy of certain pesticides and herbicides. Commonly utilized in research for creating novel bioactive molecules, especially where fluorinated compounds are needed to modulate these properties.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿495.00
inventory 250mg
10-20 days ฿3,990.00

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2-(Trifluoromethyl)-1H-indole
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antidepressants, antipsychotic drugs, antimicrobials, and anticancer agents. Its structure supports activity in central nervous system agents due to enhanced metabolic stability and binding affinity. The trifluoromethyl group improves cell permeability, lipophilicity, and bioavailability. Also employed in agrochemicals to improve the efficacy of certain pesticides and herbicides. Commonly utilized in resear

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antidepressants, antipsychotic drugs, antimicrobials, and anticancer agents. Its structure supports activity in central nervous system agents due to enhanced metabolic stability and binding affinity. The trifluoromethyl group improves cell permeability, lipophilicity, and bioavailability. Also employed in agrochemicals to improve the efficacy of certain pesticides and herbicides. Commonly utilized in research for creating novel bioactive molecules, especially where fluorinated compounds are needed to modulate these properties.

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