5-Fluoro-2-(trifluoromethyl)benzoyl Chloride
97%
- Product Code: 187501
CAS:
216144-70-6
| Molecular Weight: | 226.55 g./mol | Molecular Formula: | C₈H₃ClF₄O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00083534 | |
| Melting Point: | Boiling Point: | 169°C (Lit.) | |
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound plays a key role in introducing fluorinated benzoyl groups into larger molecules. Its high reactivity makes it valuable in the preparation of herbicides and fungicides, where the fluorine atoms enhance biological activity and stability. It is also employed in the development of active pharmaceutical ingredients, particularly in drugs targeting central nervous system disorders and inflammation. Due to the presence of both fluorine and trifluoromethyl groups, it contributes to improved metabolic resistance and membrane permeability in drug candidates. Commonly used in carbonyl coupling reactions, it reacts with amines and alcohols to form amides and esters, respectively, which are essential structural motifs in many bioactive compounds.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | ฿3,950.00 |
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5-Fluoro-2-(trifluoromethyl)benzoyl Chloride
Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound plays a key role in introducing fluorinated benzoyl groups into larger molecules. Its high reactivity makes it valuable in the preparation of herbicides and fungicides, where the fluorine atoms enhance biological activity and stability. It is also employed in the development of active pharmaceutical ingredients, particularly in drugs targeting central nervous system disorders and inflammation. Due to the presence of both fluorine and trifluoromethyl groups, it contributes to improved metabolic resistance and membrane permeability in drug candidates. Commonly used in carbonyl coupling reactions, it reacts with amines and alcohols to form amides and esters, respectively, which are essential structural motifs in many bioactive compounds.
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