4-methoxy-2,5-dimethylbenzene-1-sulfonyl chloride
97%
- Product Code: 129430
CAS:
91179-12-3
| Molecular Weight: | 234.7 g./mol | Molecular Formula: | C₉H₁₁ClO₃S |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 98-99 °C | Boiling Point: | 350.3±42.0 °C(Predicted) |
| Density: | 1.285±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, Sealed, Inert Gas |
Product Description:
Used primarily as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, this compound serves as a sulfonylating agent to introduce the 4-methoxy-2,5-dimethylbenzenesulfonyl group into target molecules. Its reactivity makes it valuable in creating sulfonamide derivatives, which are common structural motifs in bioactive compounds. It is also employed in research settings for the development of novel organic compounds, particularly in medicinal chemistry for designing enzyme inhibitors or receptor ligands. The presence of electron-donating substituents enhances the stability and selectivity during sulfonylation reactions, making it suitable for use in multi-step synthetic pathways where chemoselectivity is important.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 50mg | 10-20 days | ฿4,530.00 |
+
-
|
| 250mg | 10-20 days | ฿18,420.00 |
+
-
|
4-methoxy-2,5-dimethylbenzene-1-sulfonyl chloride
Used primarily as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, this compound serves as a sulfonylating agent to introduce the 4-methoxy-2,5-dimethylbenzenesulfonyl group into target molecules. Its reactivity makes it valuable in creating sulfonamide derivatives, which are common structural motifs in bioactive compounds. It is also employed in research settings for the development of novel organic compounds, particularly in medicinal chemistry for designing enzyme inhibitors or receptor ligands. The presence of electron-donating substituents enhances the stability and selectivity during sulfonylation reactions, making it suitable for use in multi-step synthetic pathways where chemoselectivity is important.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Purchase History for
Loading purchase history...
Cart
No products
Subtotal:
฿0.00
฿0.00
Total :