(S)-N-(2-(4-Isopropyl-4,5-dihydrooxazol-2-yl)-6-methylphenyl)methanesulfonamide
95%
- Product Code: 237444
CAS:
480444-15-3
| Molecular Weight: | 296.39 g./mol | Molecular Formula: | C₁₄H₂₀N₂O₃S |
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| EC Number: | MDL Number: | MFCD31381703 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, seal, dry, inert gas |
Product Description:
Used as a chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals where stereochemistry plays a critical role in drug efficacy. Its oxazoline core acts as a directing group in asymmetric synthesis, enabling selective carbon–carbon bond formation. Commonly employed in catalytic asymmetric alkylation or arylation reactions to construct complex molecules with high enantiomeric purity. Also serves as a ligand precursor in transition-metal-catalyzed reactions, enhancing enantioselectivity in hydrogenation and cross-coupling processes. Its sulfonamide moiety improves solubility and binding affinity in medicinal chemistry applications.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 100mg | 10-20 days | $74.00 |
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| 250mg | 10-20 days | $123.33 |
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| 1g | 10-20 days | $246.66 |
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| 5g | 10-20 days | $739.97 |
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(S)-N-(2-(4-Isopropyl-4,5-dihydrooxazol-2-yl)-6-methylphenyl)methanesulfonamide
Used as a chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals where stereochemistry plays a critical role in drug efficacy. Its oxazoline core acts as a directing group in asymmetric synthesis, enabling selective carbon–carbon bond formation. Commonly employed in catalytic asymmetric alkylation or arylation reactions to construct complex molecules with high enantiomeric purity. Also serves as a ligand precursor in transition-metal-catalyzed reactions, enhancing enantioselectivity in hydrogenation and cross-coupling processes. Its sulfonamide moiety improves solubility and binding affinity in medicinal chemistry applications.
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