3-(Trifluoromethyl)benzoyl chloride
98%
- Product Code: 117505
Alias:
3-(Trifluoromethyl)benzoyl chloride; m-trifluoromethylbenzoyl chloride
CAS:
2251-65-2
| Molecular Weight: | 208.56 g./mol | Molecular Formula: | C₈H₄ClF₃O |
|---|---|---|---|
| EC Number: | 218-844-5 | MDL Number: | MFCD00000680 |
| Melting Point: | Boiling Point: | 184-186 °C750 mm Hg(lit.) | |
| Density: | 1.383 g/mL at 25 °C(lit.) | Storage Condition: | room temperature |
Product Description:
Primarily used in organic synthesis, this compound serves as a key intermediate for the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its reactive acyl chloride group makes it valuable for introducing the 3-(trifluoromethyl)benzoyl moiety into target molecules, enhancing their biological activity or chemical properties. In pharmaceuticals, it is employed in the synthesis of active ingredients, particularly those requiring trifluoromethyl groups for improved metabolic stability and binding affinity. In agrochemicals, it contributes to the development of herbicides and pesticides with enhanced efficacy. Additionally, it finds use in the preparation of dyes, polymers, and other advanced materials, where the trifluoromethyl group imparts unique characteristics such as increased hydrophobicity or chemical resistance.
Product Specification:
| Test | Specification |
|---|---|
| Purity (GC) | 98-100 |
| Refractive Index N20/D | 1.476-1.478 |
| Specific Gravity (20/20 Degree Celsius) | 1.411-1.414 |
| Appearance | Colorless To Yellow Liquid |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿440.00 |
+
-
|
| 25.000 | 10-20 days | ฿1,110.00 |
+
-
|
| 100.000 | 10-20 days | ฿3,490.00 |
+
-
|
| 500.000 | 10-20 days | ฿14,140.00 |
+
-
|
3-(Trifluoromethyl)benzoyl chloride
Primarily used in organic synthesis, this compound serves as a key intermediate for the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its reactive acyl chloride group makes it valuable for introducing the 3-(trifluoromethyl)benzoyl moiety into target molecules, enhancing their biological activity or chemical properties. In pharmaceuticals, it is employed in the synthesis of active ingredients, particularly those requiring trifluoromethyl groups for improved metabolic stability and binding affinity. In agrochemicals, it contributes to the development of herbicides and pesticides with enhanced efficacy. Additionally, it finds use in the preparation of dyes, polymers, and other advanced materials, where the trifluoromethyl group imparts unique characteristics such as increased hydrophobicity or chemical resistance.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Cart
No products
Subtotal:
฿0.00
฿0.00
Total :