4-(Trifluoromethoxy)phenyl isothiocyanate
98%
- Product Code: 66344
CAS:
64285-95-6
| Molecular Weight: | 219.18 g./mol | Molecular Formula: | C₈H₄F₃NOS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00042412 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2~8℃, inert gas atmosphere |
Product Description:
This chemical is primarily utilized in the synthesis of various organic compounds, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the production of compounds that exhibit biological activity, such as herbicides, fungicides, and insecticides. Additionally, it is employed in the creation of small molecules for drug discovery, where it contributes to the modification of pharmacophores to enhance drug efficacy and selectivity. Its isothiocyanate group allows for the formation of thiourea derivatives, which are valuable in the study of enzyme inhibition and receptor binding. The trifluoromethoxy group enhances the lipophilicity and metabolic stability of the resulting compounds, making it a valuable component in medicinal chemistry.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 97.5 |
| SPECIFIC GRAVITY 2020 | 1.36-1.364 |
| APPEARANCE | COLORLESS TO RED-YELLOW LIQUID |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $68.10 |
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| 5.000 | 10-20 days | $222.61 |
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| 25.000 | 10-20 days | $878.23 |
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4-(Trifluoromethoxy)phenyl isothiocyanate
This chemical is primarily utilized in the synthesis of various organic compounds, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the production of compounds that exhibit biological activity, such as herbicides, fungicides, and insecticides. Additionally, it is employed in the creation of small molecules for drug discovery, where it contributes to the modification of pharmacophores to enhance drug efficacy and selectivity. Its isothiocyanate group allows for the formation of thiourea derivatives, which are valuable in the study of enzyme inhibition and receptor binding. The trifluoromethoxy group enhances the lipophilicity and metabolic stability of the resulting compounds, making it a valuable component in medicinal chemistry.
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