4-(Trifluoromethylthio)benzoyl chloride
98.0%
- Product Code: 118801
Alias:
4-(Trifluoromethylthio)benzoyl chloride; 4-(Trifluoromethylthio)benzoyl chloride; p-Trifluoromethylthiobenzoyl chloride
CAS:
330-14-3
| Molecular Weight: | 240.63 g./mol | Molecular Formula: | C₈H₄ClF₃OS |
|---|---|---|---|
| EC Number: | 000-000-0 | MDL Number: | MFCD01631632 |
| Melting Point: | Boiling Point: | 229-230 °C(lit.) | |
| Density: | 1.445 g/mL at 25 °C(lit.) | Storage Condition: | room temperature |
Product Description:
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with enhanced biological activity. Its trifluoromethylthio group is valuable for improving the metabolic stability and lipophilicity of drug molecules.
Applied in agrochemical research for creating advanced pesticides and herbicides, where the trifluoromethylthio moiety contributes to increased efficacy and resistance to degradation.
Employed in organic synthesis for the preparation of specialty chemicals, including dyes, pigments, and polymers, where it acts as a building block for introducing functional groups.
Utilized in material science for modifying surfaces or creating coatings with specific properties, such as water repellency or chemical resistance.
Its reactivity as an acyl chloride makes it a versatile reagent for coupling reactions, enabling the formation of amides, esters, and other derivatives in synthetic chemistry.
Product Specification:
| Test | Specification |
|---|---|
| Purity (GC) | 98 |
| Purity (Titration With AgNO3) | 97.5-102.5 |
| Refractive Index N20/D | 1.52-1.524 |
| Specific Gravity (20/20 Degree Celsius) | 1.44-1.445 |
| Appearance | Colorless To Yellow Liquid |
| Infrared Spectrometry | Conforms To Structure |
| Proton NMR Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿2,350.00 |
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| 5.000 | 10-20 days | ฿8,080.00 |
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4-(Trifluoromethylthio)benzoyl chloride
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with enhanced biological activity. Its trifluoromethylthio group is valuable for improving the metabolic stability and lipophilicity of drug molecules.
Applied in agrochemical research for creating advanced pesticides and herbicides, where the trifluoromethylthio moiety contributes to increased efficacy and resistance to degradation.
Employed in organic synthesis for the preparation of specialty chemicals, including dyes, pigments, and polymers, where it acts as a building block for introducing functional groups.
Utilized in material science for modifying surfaces or creating coatings with specific properties, such as water repellency or chemical resistance.
Its reactivity as an acyl chloride makes it a versatile reagent for coupling reactions, enabling the formation of amides, esters, and other derivatives in synthetic chemistry.
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