tert-Butyl 4-(2-nitro-4-(trifluoromethyl)phenyl)piperazine-1-carboxylate

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Reagent Code: #141290
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CAS Number 474329-72-1

science Other reagents with same CAS 474329-72-1

blur_circular Chemical Specifications

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Weight 375.34 g/mol
Formula C₁₆H₂₀F₃N₃O₄
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It serves as a building block for developing drug candidates targeting central nervous system disorders and inflammatory conditions. The presence of the nitro and trifluoromethyl groups enhances its utility in structure-activity relationship studies, enabling modifications to improve potency and metabolic stability. Commonly employed in medicinal chemistry for constructing piperazine-based derivatives with potential antipsychotic, antidepressant, or anticonvulsant activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,930.00
inventory 250mg
10-20 days ฿13,450.00
inventory 1g
10-20 days ฿36,300.00

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tert-Butyl 4-(2-nitro-4-(trifluoromethyl)phenyl)piperazine-1-carboxylate
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Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It serves as a building block for developing drug candidates targeting central nervous system disorders and inflammatory conditions. The presence of the nitro and trifluoromethyl groups enhances its utility in structure-activity relationship studies, enabling modifications to improve potency and metabolic stability. Commonly employed in medicinal chemistry for constructing piperazine-based

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It serves as a building block for developing drug candidates targeting central nervous system disorders and inflammatory conditions. The presence of the nitro and trifluoromethyl groups enhances its utility in structure-activity relationship studies, enabling modifications to improve potency and metabolic stability. Commonly employed in medicinal chemistry for constructing piperazine-based derivatives with potential antipsychotic, antidepressant, or anticonvulsant activity.

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