(S)-(p-Toluenesulfinyl)ferrocene
≥97%
- Product Code: 71082
CAS:
164297-25-0
| Molecular Weight: | 324.22 g./mol | Molecular Formula: | C₁₇H₁₆FeOS |
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| Density: | Storage Condition: | room temperature |
Product Description:
(S)-(p-Toluenesulfinyl)ferrocene is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. Its unique structure, combining ferrocene and a sulfinyl group, makes it highly effective in inducing chirality in various organic reactions, such as asymmetric hydrogenation, allylic alkylation, and C-H activation. This compound is also employed in the synthesis of enantiomerically pure pharmaceuticals and fine chemicals, where precise control over stereochemistry is crucial. Additionally, it serves as a valuable intermediate in the preparation of other chiral ferrocene derivatives, which are widely used in materials science and coordination chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿4,608.00 |
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(S)-(p-Toluenesulfinyl)ferrocene
(S)-(p-Toluenesulfinyl)ferrocene is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. Its unique structure, combining ferrocene and a sulfinyl group, makes it highly effective in inducing chirality in various organic reactions, such as asymmetric hydrogenation, allylic alkylation, and C-H activation. This compound is also employed in the synthesis of enantiomerically pure pharmaceuticals and fine chemicals, where precise control over stereochemistry is crucial. Additionally, it serves as a valuable intermediate in the preparation of other chiral ferrocene derivatives, which are widely used in materials science and coordination chemistry.
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