Benzyl (2S,4S)-4-hydroxypyrrolidine-2-carboxylate hydrochloride

95%

Reagent Code: #152973
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CAS Number 1864003-48-4

science Other reagents with same CAS 1864003-48-4

blur_circular Chemical Specifications

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Weight 257.71 g/mol
Formula C₁₂H₁₆ClNO₃
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used in pharmaceutical synthesis as a chiral building block for developing protease inhibitors and other bioactive molecules. Its protected hydroxyl and carboxyl groups make it valuable in peptide mimetics and drug design, particularly in creating structurally constrained analogs. Commonly employed in the preparation of antiviral and anticancer agents due to its ability to influence stereochemistry and enhance metabolic stability in final compounds. Also utilized in asymmetric synthesis where control of stereochemistry is critical.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿3,890.00
inventory 100mg
10-20 days ฿5,840.00
inventory 250mg
10-20 days ฿9,920.00
inventory 1g
10-20 days ฿32,000.00

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Benzyl (2S,4S)-4-hydroxypyrrolidine-2-carboxylate hydrochloride
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Used in pharmaceutical synthesis as a chiral building block for developing protease inhibitors and other bioactive molecules. Its protected hydroxyl and carboxyl groups make it valuable in peptide mimetics and drug design, particularly in creating structurally constrained analogs. Commonly employed in the preparation of antiviral and anticancer agents due to its ability to influence stereochemistry and enhance metabolic stability in final compounds. Also utilized in asymmetric synthesis where control of

Used in pharmaceutical synthesis as a chiral building block for developing protease inhibitors and other bioactive molecules. Its protected hydroxyl and carboxyl groups make it valuable in peptide mimetics and drug design, particularly in creating structurally constrained analogs. Commonly employed in the preparation of antiviral and anticancer agents due to its ability to influence stereochemistry and enhance metabolic stability in final compounds. Also utilized in asymmetric synthesis where control of stereochemistry is critical.

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