Ethyl (S)-5-oxotetrahydrofuran-2-carboxylate

98%

Reagent Code: #180676
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CAS Number 55094-96-7

science Other reagents with same CAS 55094-96-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 158.15 g/mol
Formula C₇H₁₀O₄
badge Registry Numbers
MDL Number MFCD00012088
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key chiral intermediate in the synthesis of active pharmaceutical ingredients, particularly in the production of anticoagulant drugs such as rivaroxaban and apixaban. Its enantiomerically pure structure enables efficient and selective reactions in multi-step organic syntheses. Commonly employed in asymmetric synthesis routes due to the presence of functional groups that allow for further transformations, including reduction, alkylation, and coupling reactions. Also utilized in the preparation of γ-amino acids and other heterocyclic compounds with biological activity. Preferred in industrial settings for its stability, solubility in common organic solvents, and compatibility with catalytic processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿18,730.00
inventory 250mg
10-20 days ฿31,820.00
inventory 1g
10-20 days ฿85,910.00

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Ethyl (S)-5-oxotetrahydrofuran-2-carboxylate
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Used as a key chiral intermediate in the synthesis of active pharmaceutical ingredients, particularly in the production of anticoagulant drugs such as rivaroxaban and apixaban. Its enantiomerically pure structure enables efficient and selective reactions in multi-step organic syntheses. Commonly employed in asymmetric synthesis routes due to the presence of functional groups that allow for further transformations, including reduction, alkylation, and coupling reactions. Also utilized in the preparation o

Used as a key chiral intermediate in the synthesis of active pharmaceutical ingredients, particularly in the production of anticoagulant drugs such as rivaroxaban and apixaban. Its enantiomerically pure structure enables efficient and selective reactions in multi-step organic syntheses. Commonly employed in asymmetric synthesis routes due to the presence of functional groups that allow for further transformations, including reduction, alkylation, and coupling reactions. Also utilized in the preparation of γ-amino acids and other heterocyclic compounds with biological activity. Preferred in industrial settings for its stability, solubility in common organic solvents, and compatibility with catalytic processes.

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