1-((2,6-Difluorophenyl)sulfonyl)-4-(naphthalen-2-ylsulfonyl)piperazine

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Reagent Code: #131277
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CAS Number 1186660-06-9

science Other reagents with same CAS 1186660-06-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 452.49 g/mol
Formula C₂₀H₁₈F₂N₂O₄S₂
thermostat Physical Properties
Boiling Point 624.7±65.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.480±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors. Its dual sulfonyl groups enhance binding selectivity, making it valuable in developing anti-inflammatory and anticancer agents. Commonly employed in structure-activity relationship (SAR) studies to optimize drug potency and metabolic stability. Also utilized in the preparation of sulfonamide-based protease inhibitors. Its rigid aromatic framework supports conformational control in drug design.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,420.00
inventory 250mg
10-20 days ฿10,920.00

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1-((2,6-Difluorophenyl)sulfonyl)-4-(naphthalen-2-ylsulfonyl)piperazine
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors. Its dual sulfonyl groups enhance binding selectivity, making it valuable in developing anti-inflammatory and anticancer agents. Commonly employed in structure-activity relationship (SAR) studies to optimize drug potency and metabolic stability. Also utilized in the preparation of sulfonamide-based protease inhibitors. Its rigid aromatic framework supports conf

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors. Its dual sulfonyl groups enhance binding selectivity, making it valuable in developing anti-inflammatory and anticancer agents. Commonly employed in structure-activity relationship (SAR) studies to optimize drug potency and metabolic stability. Also utilized in the preparation of sulfonamide-based protease inhibitors. Its rigid aromatic framework supports conformational control in drug design.

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