trans-tert-Butyl 3-(benzylamino)-4-hydroxypyrrolidine-1-carboxylate

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Reagent Code: #152814
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CAS Number 138026-89-8

science Other reagents with same CAS 138026-89-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 292.3734 g/mol
Formula C₁₆H₂₄N₂O₃
badge Registry Numbers
MDL Number MFCD09608005
inventory_2 Storage & Handling
Storage 2-8°C, drying away from light

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and other bioactive molecules. Its structural features, including the hydroxyl and amino groups in a pyrrolidine framework, make it valuable for constructing chiral building blocks in medicinal chemistry. Commonly employed in the preparation of enzyme inhibitors where stereochemistry and functional group positioning are critical for biological activity. Also utilized in research settings for the design of novel therapeutic compounds targeting neurological and metabolic disorders.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,040.00
inventory 1g
10-20 days ฿4,080.00
inventory 5g
10-20 days ฿17,700.00

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trans-tert-Butyl 3-(benzylamino)-4-hydroxypyrrolidine-1-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and other bioactive molecules. Its structural features, including the hydroxyl and amino groups in a pyrrolidine framework, make it valuable for constructing chiral building blocks in medicinal chemistry. Commonly employed in the preparation of enzyme inhibitors where stereochemistry and functional group positioning are critical for biological activity. Also utilized in research se

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and other bioactive molecules. Its structural features, including the hydroxyl and amino groups in a pyrrolidine framework, make it valuable for constructing chiral building blocks in medicinal chemistry. Commonly employed in the preparation of enzyme inhibitors where stereochemistry and functional group positioning are critical for biological activity. Also utilized in research settings for the design of novel therapeutic compounds targeting neurological and metabolic disorders.

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