4-Nitro-3-(trifluoromethyl)benzene-1-sulfonyl chloride
95%
- Product Code: 218540
CAS:
39234-83-8
| Molecular Weight: | 289.62 g./mol | Molecular Formula: | C₇H₃ClF₃NO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03094387 | |
| Melting Point: | 63 - 67 ℃ - lit. | Boiling Point: | 354.0±42.0 ℃(Predicted) |
| Density: | 1.689±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C |
Product Description:
Widely used in organic synthesis as a sulfonylating agent, particularly in the preparation of sulfonamides, which are key structural motifs in pharmaceuticals and agrochemicals. Its electron-withdrawing nitro and trifluoromethyl groups enhance reactivity, making it effective for introducing the sulfonyl group under mild conditions. Commonly employed in the development of bioactive molecules, including medicinal compounds where sulfonamide functionality imparts desired metabolic stability or binding properties. Also utilized in research settings for labeling and modifying functional groups in complex molecules due to its selective reactivity with amines and alcohols.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | ฿1,340.00 |
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| 5g | 10-20 days | ฿5,710.00 |
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| 25g | 10-20 days | ฿28,490.00 |
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4-Nitro-3-(trifluoromethyl)benzene-1-sulfonyl chloride
Widely used in organic synthesis as a sulfonylating agent, particularly in the preparation of sulfonamides, which are key structural motifs in pharmaceuticals and agrochemicals. Its electron-withdrawing nitro and trifluoromethyl groups enhance reactivity, making it effective for introducing the sulfonyl group under mild conditions. Commonly employed in the development of bioactive molecules, including medicinal compounds where sulfonamide functionality imparts desired metabolic stability or binding properties. Also utilized in research settings for labeling and modifying functional groups in complex molecules due to its selective reactivity with amines and alcohols.
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