(S)-Tetrahydrofuran-3-yl 4-methylbenzenesulfonate
98%
- Product Code: 124990
CAS:
112052-11-6
| Molecular Weight: | 242.29 g./mol | Molecular Formula: | C₁₁H₁₄O₄S |
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| EC Number: | MDL Number: | MFCD08704351 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
(S)-Tetrahydrofuran-3-yl 4-methylbenzenesulfonate is primarily utilized in organic synthesis as a chiral building block for the preparation of more complex molecules. Its structure, featuring a tetrahydrofuran ring and a tosyl group, makes it a valuable intermediate in the synthesis of pharmaceuticals and fine chemicals. The compound is often employed in asymmetric synthesis, where its chiral center is leveraged to induce stereoselectivity in reactions, leading to the production of enantiomerically pure compounds. Additionally, it serves as a precursor in the development of ligands and catalysts used in various chemical transformations, particularly in the field of medicinal chemistry where precise stereochemistry is crucial for biological activity. Its tosyl group also makes it a suitable substrate for nucleophilic substitution reactions, enabling the introduction of diverse functional groups into target molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,656.00 |
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| 0.250 | 10-20 days | ฿2,808.00 |
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| 1.000 | 10-20 days | ฿7,578.00 |
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(S)-Tetrahydrofuran-3-yl 4-methylbenzenesulfonate
(S)-Tetrahydrofuran-3-yl 4-methylbenzenesulfonate is primarily utilized in organic synthesis as a chiral building block for the preparation of more complex molecules. Its structure, featuring a tetrahydrofuran ring and a tosyl group, makes it a valuable intermediate in the synthesis of pharmaceuticals and fine chemicals. The compound is often employed in asymmetric synthesis, where its chiral center is leveraged to induce stereoselectivity in reactions, leading to the production of enantiomerically pure compounds. Additionally, it serves as a precursor in the development of ligands and catalysts used in various chemical transformations, particularly in the field of medicinal chemistry where precise stereochemistry is crucial for biological activity. Its tosyl group also makes it a suitable substrate for nucleophilic substitution reactions, enabling the introduction of diverse functional groups into target molecules.
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