2-Iodo-4-nitro-1H-indole

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Reagent Code: #200680
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CAS Number 1935958-72-7

science Other reagents with same CAS 1935958-72-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 288.04 g/mol
Formula C₈H₅IN₂O₂
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MDL Number MFCD29760711
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its structure supports functionalization in drug development, particularly in creating indole-based derivatives with potential antitumor, antimicrobial, or anti-inflammatory activity. Commonly employed in cross-coupling reactions like Suzuki or Heck reactions due to the iodo substituent, enabling carbon-carbon bond formation. Also utilized in the synthesis of fluorescent probes and dyes owing to the nitro group’s electron-withdrawing properties that influence optical characteristics.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,070.00
inventory 250mg
10-20 days ฿2,290.00
inventory 1g
10-20 days ฿7,110.00
inventory 5g
10-20 days ฿28,740.00

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2-Iodo-4-nitro-1H-indole
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its structure supports functionalization in drug development, particularly in creating indole-based derivatives with potential antitumor, antimicrobial, or anti-inflammatory activity. Commonly employed in cross-coupling reactions like Suzuki or Heck reactions due to the iodo substituent, enabling carbon-carbon bond formation. Also utilized in the synthesis of fluorescent probes and dyes owing to the nitro group’s el

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its structure supports functionalization in drug development, particularly in creating indole-based derivatives with potential antitumor, antimicrobial, or anti-inflammatory activity. Commonly employed in cross-coupling reactions like Suzuki or Heck reactions due to the iodo substituent, enabling carbon-carbon bond formation. Also utilized in the synthesis of fluorescent probes and dyes owing to the nitro group’s electron-withdrawing properties that influence optical characteristics.

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