((3,3,3-Trifluoroprop-1-en-1-yl)sulfonyl)benzene
95%
- Product Code: 112989
CAS:
105924-64-9
| Molecular Weight: | 236.21 g./mol | Molecular Formula: | C₉H₇F₃O₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00674025 | |
| Melting Point: | 68-71 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure, featuring a trifluoropropenyl group attached to a sulfonyl benzene moiety, makes it valuable for introducing fluorinated groups into target molecules. Fluorination often enhances the biological activity, stability, and metabolic resistance of compounds, which is crucial in drug design. Additionally, it serves as a key intermediate in the production of specialty chemicals, where its sulfonyl group can participate in various reactions such as nucleophilic substitutions or cross-coupling reactions. Its application extends to materials science, where it is used to modify polymers and create advanced materials with specific properties like thermal stability or chemical resistance.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,598.00 |
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| 0.250 | 10-20 days | ฿9,504.00 |
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| 1.000 | 10-20 days | ฿25,659.00 |
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((3,3,3-Trifluoroprop-1-en-1-yl)sulfonyl)benzene
This chemical is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure, featuring a trifluoropropenyl group attached to a sulfonyl benzene moiety, makes it valuable for introducing fluorinated groups into target molecules. Fluorination often enhances the biological activity, stability, and metabolic resistance of compounds, which is crucial in drug design. Additionally, it serves as a key intermediate in the production of specialty chemicals, where its sulfonyl group can participate in various reactions such as nucleophilic substitutions or cross-coupling reactions. Its application extends to materials science, where it is used to modify polymers and create advanced materials with specific properties like thermal stability or chemical resistance.
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