The isocyanate readily reacts with amines and alcohols to form ureas and carbamates, while the trifluoromethyl group strongly influences electronic properties, lipophilicity, and metabolic stability in downstream products. 1-Chloro-4-isocyanato-2-(trifluoromethyl)benzene is a highly reactive aromatic isocyanate used as a synthetic intermediate in pharmaceutical, agrochemical, and materials chemistry.It consists of a chlorinated, trifluoromethyl-substituted benzene ring bearing an isocyanate (–N=C=O) functional group, which is the key reactive site.
1-Chloro-4-isocyanato-2-(trifluoromethyl) benzene
| API Name | Regorafenib |
|---|---|
| CAS No | 327-78-6 |
| Molecular Formula | C8H3ClF3NO |
| Molecular Weight | 221.56 g/mol |
| Synonyms | 1-chloro-4-isocyanato-2-(trifluoromethyl)benzene |
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Frequently Asked Questions
The isocyanate readily reacts with amines and alcohols to form ureas and carbamates, while the trifluoromethyl group strongly influences electronic properties, lipophilicity, and metabolic stability in downstream products. 1-Chloro-4-isocyanato-2-(trifluoromethyl)benzene is a highly reactive aromatic isocyanate used as a synthetic intermediate in pharmaceutical, agrochemical, and materials chemistry.It consists of a chlorinated, trifluoromethyl-substituted benzene ring bearing an isocyanate (–N=C=O) functional group, which is the key reactive site.
The CAS number of 1-Chloro-4-isocyanato-2-(trifluoromethyl) benzene is 327-78-6.
The molecular formula of 1-Chloro-4-isocyanato-2-(trifluoromethyl) benzene is C8H3ClF3NO.
The listed molecular weight of 1-Chloro-4-isocyanato-2-(trifluoromethyl) benzene is 221.56 g/mol.
1-Chloro-4-isocyanato-2-(trifluoromethyl) benzene is listed as being used in connection with the following API: Regorafenib.
The listed synonym or IUPAC name for 1-Chloro-4-isocyanato-2-(trifluoromethyl) benzene is 1-chloro-4-isocyanato-2-(trifluoromethyl)benzene.