1-(4-Nitro-2-(trifluoromethyl)phenyl)piperazine

95%

Reagent Code: #217273
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CAS Number 381242-61-1

science Other reagents with same CAS 381242-61-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 275.23 g/mol
Formula C₁₁H₁₂F₃N₃O₂
badge Registry Numbers
MDL Number MFCD01933012
thermostat Physical Properties
Melting Point 54-55°C
Boiling Point 382.1°C
inventory_2 Storage & Handling
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 antipsychotic, antidepressant, or antihistaminic properties. Its structure supports binding to central nervous system receptors, making it valuable in medicinal chemistry research. Also employed in the preparation of novel piperazine-based derivatives for structure-activity relationship (SAR) studies. Additionally, it serves as a building block in the creation of fluorinated organic compounds, where the trifluoromethyl group enhances metabolic stability and lipophilicity in drug candidates.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿550.00
1-(4-Nitro-2-(trifluoromethyl)phenyl)piperazine
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Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential antipsychotic, antidepressant, or antihistaminic properties. Its structure supports binding to central nervous system receptors, making it valuable in medicinal chemistry research. Also employed in the preparation of novel piperazine-based derivatives for structure-activity relationship (SAR) studies. Additionally, it serves as a building block in the creat

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential antipsychotic, antidepressant, or antihistaminic properties. Its structure supports binding to central nervous system receptors, making it valuable in medicinal chemistry research. Also employed in the preparation of novel piperazine-based derivatives for structure-activity relationship (SAR) studies. Additionally, it serves as a building block in the creation of fluorinated organic compounds, where the trifluoromethyl group enhances metabolic stability and lipophilicity in drug candidates.

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