1-Ethyl-7-(trifluoromethyl)-1,2,3,4-tetrahydroquinoline

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Reagent Code: #184835
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CAS Number 2288709-48-6

science Other reagents with same CAS 2288709-48-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.245 g/mol
Formula C₁₂H₁₄F₃N
badge Registry Numbers
MDL Number MFCD31715104
thermostat Physical Properties
Boiling Point 284.2±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.155±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. Its structure supports activity in modulating neurological receptors, making it valuable in research for antidepressants and antipsychotic drugs. Also employed in agrochemical research for designing novel pesticides due to the stability and bioavailability imparted by the trifluoromethyl group. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿65,120.00

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1-Ethyl-7-(trifluoromethyl)-1,2,3,4-tetrahydroquinoline
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. Its structure supports activity in modulating neurological receptors, making it valuable in research for antidepressants and antipsychotic drugs. Also employed in agrochemical research for designing novel pesticides due to the stability and bioavailability imparted by the trifluoromethyl group. Commonly utilized in medicinal chemistry for structure-activity relationship

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. Its structure supports activity in modulating neurological receptors, making it valuable in research for antidepressants and antipsychotic drugs. Also employed in agrochemical research for designing novel pesticides due to the stability and bioavailability imparted by the trifluoromethyl group. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates.

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