(S)-3-Methyl-1-((4-(trifluoromethyl)phenyl)sulfonyl)piperazine

98%

Reagent Code: #237695
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CAS Number 1204535-11-4

science Other reagents with same CAS 1204535-11-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 308.32 g/mol
Formula C₁₂H₁₅F₃N₂O₂S
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting central nervous system disorders such as antidepressants and mood stabilizers. Its structure, featuring a sulfonyl piperazine with a trifluoromethyl-substituted phenyl group, supports the development of selective receptor modulators, especially for serotonin and dopamine receptors, by enhancing blood-brain barrier penetration and receptor specificity. Commonly employed in medicinal chemistry for optimizing drug candidates due to its favorable conformational and electronic properties. Also utilized in the preparation of chiral catalysts and asymmetric synthesis applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,690.00
(S)-3-Methyl-1-((4-(trifluoromethyl)phenyl)sulfonyl)piperazine
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Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting central nervous system disorders such as antidepressants and mood stabilizers. Its structure, featuring a sulfonyl piperazine with a trifluoromethyl-substituted phenyl group, supports the development of selective receptor modulators, especially for serotonin and dopamine receptors, by enhancing blood-brain barrier penetration and receptor specificity. Commonly employed in medicinal

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting central nervous system disorders such as antidepressants and mood stabilizers. Its structure, featuring a sulfonyl piperazine with a trifluoromethyl-substituted phenyl group, supports the development of selective receptor modulators, especially for serotonin and dopamine receptors, by enhancing blood-brain barrier penetration and receptor specificity. Commonly employed in medicinal chemistry for optimizing drug candidates due to its favorable conformational and electronic properties. Also utilized in the preparation of chiral catalysts and asymmetric synthesis applications.

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