4-Iodo-1-nitro-2-(trifluoromethyl)benzene
≥95%
- Product Code: 201269
CAS:
393-10-2
| Molecular Weight: | 317 g./mol | Molecular Formula: | C₇H₃F₃INO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08282788 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in reactions involving cross-coupling such as Suzuki or Heck reactions due to the presence of the iodine moiety. The electron-withdrawing nitro and trifluoromethyl groups enhance reactivity in nucleophilic aromatic substitution and facilitate the preparation of more complex aromatic compounds. Commonly employed in the development of fluorinated bioactive molecules, where the trifluoromethyl group contributes to metabolic stability and lipophilicity. Also utilized in the manufacture of specialty chemicals requiring high selectivity and reactivity in multi-step organic syntheses.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 5g | 10-20 days | ฿21,820.00 |
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4-Iodo-1-nitro-2-(trifluoromethyl)benzene
Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in reactions involving cross-coupling such as Suzuki or Heck reactions due to the presence of the iodine moiety. The electron-withdrawing nitro and trifluoromethyl groups enhance reactivity in nucleophilic aromatic substitution and facilitate the preparation of more complex aromatic compounds. Commonly employed in the development of fluorinated bioactive molecules, where the trifluoromethyl group contributes to metabolic stability and lipophilicity. Also utilized in the manufacture of specialty chemicals requiring high selectivity and reactivity in multi-step organic syntheses.
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