(2S,4S)-tert-Butyl 2-(hydroxymethyl)-4-methylpyrrolidine-1-carboxylate

95%

Reagent Code: #236173
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CAS Number 540501-56-2

science Other reagents with same CAS 540501-56-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.29 g/mol
Formula C₁₁H₂₁NO₃
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MDL Number MFCD22421683
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active molecules. Its stereochemistry makes it valuable for creating structurally defined intermediates in drug discovery. Commonly employed in asymmetric synthesis to introduce specific stereocenters in complex molecules. Also utilized in the preparation of peptidomimetics due to its rigid pyrrolidine scaffold and functional handles for further derivatization.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,720.00
inventory 250mg
10-20 days ฿12,000.00
(2S,4S)-tert-Butyl 2-(hydroxymethyl)-4-methylpyrrolidine-1-carboxylate
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active molecules. Its stereochemistry makes it valuable for creating structurally defined intermediates in drug discovery. Commonly employed in asymmetric synthesis to introduce specific stereocenters in complex molecules. Also utilized in the preparation of peptidomimetics due to its rigid pyrrolidine scaffold and functional handles for further derivatization.
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active molecules. Its stereochemistry makes it valuable for creating structurally defined intermediates in drug discovery. Commonly employed in asymmetric synthesis to introduce specific stereocenters in complex molecules. Also utilized in the preparation of peptidomimetics due to its rigid pyrrolidine scaffold and functional handles for further derivatization.
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