3-Iodo-1-(phenylsulfonyl)-1H-indole

95%

Reagent Code: #200623
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CAS Number 80360-14-1

science Other reagents with same CAS 80360-14-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 383.20 g/mol
Formula C₁₄H₁₀INO₂S
badge Registry Numbers
MDL Number MFCD09037474
thermostat Physical Properties
Melting Point 125-129 °C
Boiling Point 516.55 °C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, preserved from light, dry sealed

description Product Description

Used as a key intermediate in the synthesis of biologically active indole derivatives, particularly in pharmaceutical research. Its structure allows for selective functionalization at the 3-position, making it valuable in the development of indole-based drugs. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to construct complex heterocyclic systems. Also utilized in the preparation of serotonin receptor ligands and other neuroactive compounds due to the indole core’s prevalence in central nervous system agents. Its sulfonyl and iodo groups provide orthogonal reactivity, enabling stepwise modifications in multi-step synthetic routes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,690.00
inventory 250mg
10-20 days ฿3,090.00
inventory 1g
10-20 days ฿6,170.00

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3-Iodo-1-(phenylsulfonyl)-1H-indole
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Used as a key intermediate in the synthesis of biologically active indole derivatives, particularly in pharmaceutical research. Its structure allows for selective functionalization at the 3-position, making it valuable in the development of indole-based drugs. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to construct complex heterocyclic systems. Also utilized in the preparation of serotonin receptor ligands and other neuroactive compounds due to the indole core’s preval

Used as a key intermediate in the synthesis of biologically active indole derivatives, particularly in pharmaceutical research. Its structure allows for selective functionalization at the 3-position, making it valuable in the development of indole-based drugs. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to construct complex heterocyclic systems. Also utilized in the preparation of serotonin receptor ligands and other neuroactive compounds due to the indole core’s prevalence in central nervous system agents. Its sulfonyl and iodo groups provide orthogonal reactivity, enabling stepwise modifications in multi-step synthetic routes.

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