(4S)-4-Benzyl-3-[(1S,2R)-2-hydroxy-3-cyclopenten-1-yl]carbonyl-1,3-oxazolidin-2-one

95%

Reagent Code: #235997
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CAS Number 178327-18-9

science Other reagents with same CAS 178327-18-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.31 g/mol
Formula C₁₆H₁₇NO₄
inventory_2 Storage & Handling
Storage 2-8°C, dry, closed

description Product Description

Used in pharmaceutical synthesis as a chiral auxiliary or intermediate in the development of biologically active compounds. Its structural features, including the oxazolidinone ring and hydroxy-substituted cyclopentane, make it valuable for asymmetric induction in stereoselective reactions. Commonly employed in the preparation of complex molecules requiring high enantiomeric purity, particularly in the research of enzyme inhibitors and antiviral agents. Also utilized in the optimization of synthetic routes where stereochemical control is critical.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿32,600.00
(4S)-4-Benzyl-3-[(1S,2R)-2-hydroxy-3-cyclopenten-1-yl]carbonyl-1,3-oxazolidin-2-one
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Used in pharmaceutical synthesis as a chiral auxiliary or intermediate in the development of biologically active compounds. Its structural features, including the oxazolidinone ring and hydroxy-substituted cyclopentane, make it valuable for asymmetric induction in stereoselective reactions. Commonly employed in the preparation of complex molecules requiring high enantiomeric purity, particularly in the research of enzyme inhibitors and antiviral agents. Also utilized in the optimization of synthetic rout

Used in pharmaceutical synthesis as a chiral auxiliary or intermediate in the development of biologically active compounds. Its structural features, including the oxazolidinone ring and hydroxy-substituted cyclopentane, make it valuable for asymmetric induction in stereoselective reactions. Commonly employed in the preparation of complex molecules requiring high enantiomeric purity, particularly in the research of enzyme inhibitors and antiviral agents. Also utilized in the optimization of synthetic routes where stereochemical control is critical.

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