(S)-N-(2-(4-Isopropyl-4,5-dihydrooxazol-2-yl)-6-methylphenyl)methanesulfonamide

95%

Reagent Code: #237444
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CAS Number 480444-15-3

science Other reagents with same CAS 480444-15-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.39 g/mol
Formula C₁₄H₂₀N₂O₃S
badge Registry Numbers
MDL Number MFCD31381703
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, inert gas

description 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.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,400.00
inventory 250mg
10-20 days ฿4,000.00
inventory 1g
10-20 days ฿8,000.00
inventory 5g
10-20 days ฿24,000.00
(S)-N-(2-(4-Isopropyl-4,5-dihydrooxazol-2-yl)-6-methylphenyl)methanesulfonamide
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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, enhan
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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