N-Sulfinyl-p-toluenesulfonamide
≥70%
- Product Code: 121480
CAS:
4104-47-6
Molecular Weight: | 217.26 g./mol | Molecular Formula: | C₇H₇NO₃S₂ |
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EC Number: | MDL Number: | MFCD00082512 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | -20°C |
Product Description:
N-Sulfinyl-p-toluenesulfonamide is primarily used as a versatile reagent in organic synthesis, particularly in the formation of sulfonamides and sulfinamides. It serves as a key intermediate in the preparation of various pharmaceutical compounds, enabling the introduction of sulfonamide functional groups into target molecules. This chemical is also employed in asymmetric synthesis, where it acts as a chiral auxiliary to induce stereoselectivity in reactions, leading to the production of enantiomerically pure compounds. Additionally, it is utilized in the development of peptidomimetics and other biologically active molecules, making it valuable in drug discovery and medicinal chemistry research. Its stability and reactivity under mild conditions further enhance its applicability in complex synthetic pathways.
Product Specification:
Test | Specification |
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Appearance | Light Yellow To Amber To Dark Green Powder To Crystal |
Purity (%) | 70-100 |
Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.200 | 10-20 days | ฿2,360.00 |
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1.000 | 10-20 days | ฿8,450.00 |
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N-Sulfinyl-p-toluenesulfonamide
N-Sulfinyl-p-toluenesulfonamide is primarily used as a versatile reagent in organic synthesis, particularly in the formation of sulfonamides and sulfinamides. It serves as a key intermediate in the preparation of various pharmaceutical compounds, enabling the introduction of sulfonamide functional groups into target molecules. This chemical is also employed in asymmetric synthesis, where it acts as a chiral auxiliary to induce stereoselectivity in reactions, leading to the production of enantiomerically pure compounds. Additionally, it is utilized in the development of peptidomimetics and other biologically active molecules, making it valuable in drug discovery and medicinal chemistry research. Its stability and reactivity under mild conditions further enhance its applicability in complex synthetic pathways.
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