(2R,4R)-4-Hydroxypyrrolidine-2-carboxamide hydrochloride

98%

Reagent Code: #231278
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CAS Number 1844171-46-5

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 166.61 g/mol
Formula C₅H₁₁ClN₂O₂
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 rigid pyrrolidine backbone and functional groups make it valuable in drug design, particularly for targeting enzymes involved in metabolic and neurological pathways. Commonly employed in the preparation of antiviral and antidiabetic agents due to its ability to mimic natural amino acid structures and enhance binding selectivity. Also utilized in asymmetric synthesis to introduce stereochemical control in complex molecule construction.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,210.00
inventory 250mg
10-20 days ฿10,500.00
inventory 1g
10-20 days ฿32,240.00
(2R,4R)-4-Hydroxypyrrolidine-2-carboxamide hydrochloride
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Used in pharmaceutical synthesis as a chiral building block for developing protease inhibitors and other bioactive molecules. Its rigid pyrrolidine backbone and functional groups make it valuable in drug design, particularly for targeting enzymes involved in metabolic and neurological pathways. Commonly employed in the preparation of antiviral and antidiabetic agents due to its ability to mimic natural amino acid structures and enhance binding selectivity. Also utilized in asymmetric synthesis to introdu

Used in pharmaceutical synthesis as a chiral building block for developing protease inhibitors and other bioactive molecules. Its rigid pyrrolidine backbone and functional groups make it valuable in drug design, particularly for targeting enzymes involved in metabolic and neurological pathways. Commonly employed in the preparation of antiviral and antidiabetic agents due to its ability to mimic natural amino acid structures and enhance binding selectivity. Also utilized in asymmetric synthesis to introduce stereochemical control in complex molecule construction.

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