3-(Pentafluorosulfanyl)benzaldehyde
97%
- Product Code: 227592
CAS:
401892-80-6
| Molecular Weight: | 232.17 g./mol | Molecular Formula: | C₇H₅F₅OS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03788517 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Used primarily as a specialty intermediate in the synthesis of fluorinated organic compounds, particularly in pharmaceuticals and agrochemicals where high lipophilicity and metabolic stability are desired. Its pentafluorosulfanyl group imparts strong electron-withdrawing properties, making it valuable in the development of bioactive molecules with enhanced membrane permeability and resistance to oxidative degradation. It is also employed in materials science for designing novel fluorinated polymers and liquid crystals with unique thermal and dielectric properties. Due to the stability and distinct polarity of the SF5 group, this compound supports research in medicinal chemistry for structure-activity relationship studies, especially in aromatic systems targeting enzyme inhibitors or receptor ligands.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿2,820.00 |
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| 1g | 10-20 days | ฿8,050.00 |
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3-(Pentafluorosulfanyl)benzaldehyde
Used primarily as a specialty intermediate in the synthesis of fluorinated organic compounds, particularly in pharmaceuticals and agrochemicals where high lipophilicity and metabolic stability are desired. Its pentafluorosulfanyl group imparts strong electron-withdrawing properties, making it valuable in the development of bioactive molecules with enhanced membrane permeability and resistance to oxidative degradation. It is also employed in materials science for designing novel fluorinated polymers and liquid crystals with unique thermal and dielectric properties. Due to the stability and distinct polarity of the SF5 group, this compound supports research in medicinal chemistry for structure-activity relationship studies, especially in aromatic systems targeting enzyme inhibitors or receptor ligands.
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