N-(2-Iodophenyl)-4-methylbenzenesulfonamide

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Reagent Code: #219162
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CAS Number 61613-20-5

science Other reagents with same CAS 61613-20-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 373.21 g/mol
Formula C₁₃H₁₂INO₂S
badge Registry Numbers
MDL Number MFCD00574370
thermostat Physical Properties
Melting Point 90-92 °C
Boiling Point 443.4±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.720±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof storage, dry seal

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of bioactive molecules and pharmaceuticals. Its structure allows for participation in coupling reactions, making it valuable in the development of sulfonamide-based drugs. Commonly employed in research settings to construct complex heterocyclic systems through intramolecular cyclization or palladium-catalyzed reactions. Also finds use in the design of enzyme inhibitors due to the sulfonamide functional group's affinity for certain biological targets.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,720.00
inventory 500mg
10-20 days ฿3,940.00
inventory 1g
10-20 days ฿6,740.00
inventory 5g
10-20 days ฿26,390.00
inventory 250mg
10-20 days ฿2,440.00

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N-(2-Iodophenyl)-4-methylbenzenesulfonamide
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Used as an intermediate in organic synthesis, particularly in the preparation of bioactive molecules and pharmaceuticals. Its structure allows for participation in coupling reactions, making it valuable in the development of sulfonamide-based drugs. Commonly employed in research settings to construct complex heterocyclic systems through intramolecular cyclization or palladium-catalyzed reactions. Also finds use in the design of enzyme inhibitors due to the sulfonamide functional group's affinity for cert

Used as an intermediate in organic synthesis, particularly in the preparation of bioactive molecules and pharmaceuticals. Its structure allows for participation in coupling reactions, making it valuable in the development of sulfonamide-based drugs. Commonly employed in research settings to construct complex heterocyclic systems through intramolecular cyclization or palladium-catalyzed reactions. Also finds use in the design of enzyme inhibitors due to the sulfonamide functional group's affinity for certain biological targets.

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