Tert-butyl(S)-3-(trifluoromethyl)piperazine-1-carboxylate

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Reagent Code: #244568
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CAS Number 1240587-95-4

science Other reagents with same CAS 1240587-95-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.25 g/mol
Formula C₁₀H₁₇F₃N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its chiral piperazine backbone with trifluoromethyl group makes it valuable in developing potent and selective receptor modulators. Commonly employed in medicinal chemistry for structure-activity relationship studies, especially in the development of antidepressants, antipsychotics, and kinase inhibitors. The tert-butyl carbamate (Boc) group allows for easy protection and deprotection during multi-step syntheses, enhancing its utility in drug discovery.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿76,360.00
inventory 250mg
10-20 days ฿24,620.00
inventory 100mg
10-20 days ฿14,040.00
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Tert-butyl(S)-3-(trifluoromethyl)piperazine-1-carboxylate
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Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its chiral piperazine backbone with trifluoromethyl group makes it valuable in developing potent and selective receptor modulators. Commonly employed in medicinal chemistry for structure-activity relationship studies, especially in the development of antidepressants, antipsychotics, and kinase inhibitors. The tert-butyl carbamate (Boc) group allows for eas

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its chiral piperazine backbone with trifluoromethyl group makes it valuable in developing potent and selective receptor modulators. Commonly employed in medicinal chemistry for structure-activity relationship studies, especially in the development of antidepressants, antipsychotics, and kinase inhibitors. The tert-butyl carbamate (Boc) group allows for easy protection and deprotection during multi-step syntheses, enhancing its utility in drug discovery.

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