1-((4-Nitrophenyl)sulfonyl)piperidine

95%

Reagent Code: #219241
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CAS Number 64268-93-5

science Other reagents with same CAS 64268-93-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 270.31 g/mol
Formula C₁₁H₁₄N₂O₄S
badge Registry Numbers
MDL Number MFCD00276970
thermostat Physical Properties
Melting Point 166 °C
Boiling Point 435.9 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of sulfonamide-based pharmaceuticals. It serves as a building block in the development of bioactive molecules, including potential protease inhibitors and antimicrobial agents. Its nitro group allows for further functionalization through reduction to an amine, enabling conjugation in multi-step syntheses. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its stable sulfonyl linker and aromatic polarity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,380.00
inventory 250mg
10-20 days ฿8,690.00
inventory 1g
10-20 days ฿26,050.00

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1-((4-Nitrophenyl)sulfonyl)piperidine
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Used as an intermediate in organic synthesis, particularly in the preparation of sulfonamide-based pharmaceuticals. It serves as a building block in the development of bioactive molecules, including potential protease inhibitors and antimicrobial agents. Its nitro group allows for further functionalization through reduction to an amine, enabling conjugation in multi-step syntheses. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its stable sulfonyl linker and a

Used as an intermediate in organic synthesis, particularly in the preparation of sulfonamide-based pharmaceuticals. It serves as a building block in the development of bioactive molecules, including potential protease inhibitors and antimicrobial agents. Its nitro group allows for further functionalization through reduction to an amine, enabling conjugation in multi-step syntheses. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its stable sulfonyl linker and aromatic polarity.

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