(S)-(p-Toluenesulfinyl)ferrocene

≥97%

Reagent Code: #71082
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CAS Number 164297-25-0

science Other reagents with same CAS 164297-25-0

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Weight 324.22 g/mol
Formula C₁₇H₁₆FeOS
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description 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.

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inventory 250mg
10-20 days ฿4,608.00

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(S)-(p-Toluenesulfinyl)ferrocene
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(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 pr

(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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