2, 6-Dimethoxybenzene-1-sulfonyl chloride
97%
- Product Code: 177883
CAS:
145980-89-8
| Molecular Weight: | 236.67 g./mol | Molecular Formula: | C₈H₉ClO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18395734 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry |
Product Description:
Widely used as a sulfonylating agent in organic synthesis, particularly in the preparation of sulfonamides and sulfonate esters. Its reactivity makes it valuable for introducing the 2,6-dimethoxybenzenesulfonyl (DMS) group, which acts as a protecting group for amines due to its stability under various reaction conditions. The DMS-protected amines are especially useful in peptide synthesis and other multi-step syntheses where selective deprotection is required. It is also employed in the development of pharmaceuticals and agrochemicals, where controlled functionalization of nitrogen-containing compounds is critical. The compound’s steric and electronic properties enhance selectivity in sulfonylation reactions, improving yield and purity in complex molecule assembly.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿820.00 |
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| 1g | 10-20 days | ฿2,080.00 |
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| 5g | 10-20 days | ฿8,330.00 |
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| 25g | 10-20 days | ฿35,020.00 |
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2, 6-Dimethoxybenzene-1-sulfonyl chloride
Widely used as a sulfonylating agent in organic synthesis, particularly in the preparation of sulfonamides and sulfonate esters. Its reactivity makes it valuable for introducing the 2,6-dimethoxybenzenesulfonyl (DMS) group, which acts as a protecting group for amines due to its stability under various reaction conditions. The DMS-protected amines are especially useful in peptide synthesis and other multi-step syntheses where selective deprotection is required. It is also employed in the development of pharmaceuticals and agrochemicals, where controlled functionalization of nitrogen-containing compounds is critical. The compound’s steric and electronic properties enhance selectivity in sulfonylation reactions, improving yield and purity in complex molecule assembly.
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