N-(4-Iodophenyl)-4-methylbenzenesulfonamide

95%

Reagent Code: #219232
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CAS Number 158268-30-5

science Other reagents with same CAS 158268-30-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 373.21 g/mol
Formula C₁₃H₁₂INO₂S
thermostat Physical Properties
Melting Point 96 °C
Boiling Point 446.5±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.720±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of sulfonamide-based pharmaceuticals. It serves in the development of bioactive molecules due to the presence of both iodine and sulfonamide functional groups, which are common in medicinal chemistry. The compound is also employed in cross-coupling reactions, such as Suzuki or Heck reactions, where the iodophenyl group acts as a reactive site for forming carbon-carbon bonds. Its structure makes it useful in the design of enzyme inhibitors and in the synthesis of functionalized aromatic compounds for research in drug discovery and materials science.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,580.00
inventory 250mg
10-20 days ฿4,720.00
inventory 1g
10-20 days ฿11,880.00
N-(4-Iodophenyl)-4-methylbenzenesulfonamide
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Used as an intermediate in organic synthesis, particularly in the preparation of sulfonamide-based pharmaceuticals. It serves in the development of bioactive molecules due to the presence of both iodine and sulfonamide functional groups, which are common in medicinal chemistry. The compound is also employed in cross-coupling reactions, such as Suzuki or Heck reactions, where the iodophenyl group acts as a reactive site for forming carbon-carbon bonds. Its structure makes it useful in the design of enzyme

Used as an intermediate in organic synthesis, particularly in the preparation of sulfonamide-based pharmaceuticals. It serves in the development of bioactive molecules due to the presence of both iodine and sulfonamide functional groups, which are common in medicinal chemistry. The compound is also employed in cross-coupling reactions, such as Suzuki or Heck reactions, where the iodophenyl group acts as a reactive site for forming carbon-carbon bonds. Its structure makes it useful in the design of enzyme inhibitors and in the synthesis of functionalized aromatic compounds for research in drug discovery and materials science.

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