(S,E)-N-(2-((tert-Butyldimethylsilyl)oxy)ethylidene)-2-methylpropane-2-sulfinamide
95%
- Product Code: 123729
CAS:
918413-70-4
| Molecular Weight: | 277.5 g./mol | Molecular Formula: | C₁₂H₂₇NO₂SSi |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18252944 | |
| Melting Point: | Boiling Point: | 323.1±44.0 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, inert gas |
Product Description:
This compound is primarily utilized in organic synthesis as a chiral auxiliary or reagent, particularly in asymmetric synthesis to induce stereoselectivity in chemical reactions. It is often employed in the preparation of enantiomerically pure compounds, such as pharmaceuticals or complex natural products, by facilitating the formation of specific stereocenters. The tert-butyldimethylsilyl (TBS) protecting group enhances the stability of the intermediate during reactions, while the sulfinamide moiety acts as a directing group to control the stereochemistry of nucleophilic additions. Its application is particularly valuable in the synthesis of bioactive molecules, where precise control over molecular configuration is critical for efficacy and function.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $122.05 |
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| 0.250 | 10-20 days | $207.65 |
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| 1.000 | 10-20 days | $559.77 |
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(S,E)-N-(2-((tert-Butyldimethylsilyl)oxy)ethylidene)-2-methylpropane-2-sulfinamide
This compound is primarily utilized in organic synthesis as a chiral auxiliary or reagent, particularly in asymmetric synthesis to induce stereoselectivity in chemical reactions. It is often employed in the preparation of enantiomerically pure compounds, such as pharmaceuticals or complex natural products, by facilitating the formation of specific stereocenters. The tert-butyldimethylsilyl (TBS) protecting group enhances the stability of the intermediate during reactions, while the sulfinamide moiety acts as a directing group to control the stereochemistry of nucleophilic additions. Its application is particularly valuable in the synthesis of bioactive molecules, where precise control over molecular configuration is critical for efficacy and function.
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