2-Iodo-4-nitro-1H-indole
96%
- Product Code: 200680
CAS:
1935958-72-7
| Molecular Weight: | 288.04 g./mol | Molecular Formula: | C₈H₅IN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD29760711 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, seal, dry |
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.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿1,070.00 |
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| 250mg | 10-20 days | ฿2,290.00 |
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| 1g | 10-20 days | ฿7,110.00 |
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| 5g | 10-20 days | ฿28,740.00 |
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2-Iodo-4-nitro-1H-indole
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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