3-(Trifluoromethyl)dibenzo[b,e]oxepin-11(6H)-one

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Reagent Code: #240773
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CAS Number 4504-94-3

science Other reagents with same CAS 4504-94-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.23 g/mol
Formula C₁₅H₉F₃O₂
thermostat Physical Properties
Boiling Point 394.2±42.0°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily in pharmaceutical research as a key intermediate in the synthesis of bioactive compounds, particularly in the development of antipsychotic and antidepressant drugs. Its rigid tricyclic structure with a trifluoromethyl substituent enhances metabolic stability and binding selectivity to central nervous system receptors. This compound is also explored in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate dopamine and serotonin pathways. Additionally, it serves as a building block in the design of novel heterocyclic systems for drug discovery.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,010.00
inventory 250mg
10-20 days ฿6,600.00

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3-(Trifluoromethyl)dibenzo[b,e]oxepin-11(6H)-one
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Used primarily in pharmaceutical research as a key intermediate in the synthesis of bioactive compounds, particularly in the development of antipsychotic and antidepressant drugs. Its rigid tricyclic structure with a trifluoromethyl substituent enhances metabolic stability and binding selectivity to central nervous system receptors. This compound is also explored in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate dopamine and serotonin pathways. Additi

Used primarily in pharmaceutical research as a key intermediate in the synthesis of bioactive compounds, particularly in the development of antipsychotic and antidepressant drugs. Its rigid tricyclic structure with a trifluoromethyl substituent enhances metabolic stability and binding selectivity to central nervous system receptors. This compound is also explored in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate dopamine and serotonin pathways. Additionally, it serves as a building block in the design of novel heterocyclic systems for drug discovery.

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