(S)-tert-Butyl 3-oxotetrahydro-1H-oxazolo[3,4-a]pyrazine-7(3H)-carboxylate

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Reagent Code: #236181
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CAS Number 958635-18-2

science Other reagents with same CAS 958635-18-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.27 g/mol
Formula C₁₁H₁₈N₂O₄
badge Registry Numbers
MDL Number MFCD17676345
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used as a chiral intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals targeting central nervous system disorders. Its structure supports the formation of peptidomimetics, making it valuable in medicinal chemistry for designing enzyme inhibitors. Commonly employed in asymmetric synthesis due to the preserved stereochemistry, enabling high enantioselectivity in final drug candidates. Also utilized in research settings for constructing constrained heterocyclic scaffolds in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿430.00
inventory 250mg
10-20 days ฿720.00
(S)-tert-Butyl 3-oxotetrahydro-1H-oxazolo[3,4-a]pyrazine-7(3H)-carboxylate
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Used as a chiral intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals targeting central nervous system disorders. Its structure supports the formation of peptidomimetics, making it valuable in medicinal chemistry for designing enzyme inhibitors. Commonly employed in asymmetric synthesis due to the preserved stereochemistry, enabling high enantioselectivity in final drug candidates. Also utilized in research settings for constructing constraine

Used as a chiral intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals targeting central nervous system disorders. Its structure supports the formation of peptidomimetics, making it valuable in medicinal chemistry for designing enzyme inhibitors. Commonly employed in asymmetric synthesis due to the preserved stereochemistry, enabling high enantioselectivity in final drug candidates. Also utilized in research settings for constructing constrained heterocyclic scaffolds in drug discovery programs.

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