1-(2-Fluoro-4-nitrophenyl)piperazine

98%

Reagent Code: #188730
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CAS Number 154590-33-7

science Other reagents with same CAS 154590-33-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.22 g/mol
Formula C₁₀H₁₂FN₃O₂
badge Registry Numbers
MDL Number MFCD01572463
thermostat Physical Properties
Melting Point 70-73 °C
Boiling Point 392.728 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry, light-proof

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) for central nervous system (CNS) agents. It serves as a building block in the preparation of selective receptor modulators, including serotonin and dopamine receptor ligands. Its structure facilitates the creation of more complex molecules with potential antipsychotic, antidepressant, or anxiolytic activity. Commonly employed in medicinal chemistry research for structure-activity relationship (SAR) studies due to the presence of both electron-withdrawing nitro and fluorine groups, which influence binding affinity and metabolic stability. Also utilized in the preparation of fluorescent probes and labeled compounds for biochemical assays.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,810.00
inventory 5g
10-20 days ฿8,910.00
inventory 25g
10-20 days ฿38,610.00

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1-(2-Fluoro-4-nitrophenyl)piperazine
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Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) for central nervous system (CNS) agents. It serves as a building block in the preparation of selective receptor modulators, including serotonin and dopamine receptor ligands. Its structure facilitates the creation of more complex molecules with potential antipsychotic, antidepressant, or anxiolytic activity. Commonly employed in medicinal chemistry research for structure-activity relationship (SAR) studies due to the presence of both electron-withdrawing nitro and fluorine groups, which influence binding affinity and metabolic stability. Also utilized in the preparation of fluorescent probes and labeled compounds for biochemical assays.
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