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

98%

Reagent Code: #236150
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CAS Number 477293-60-0

science Other reagents with same CAS 477293-60-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.26 g/mol
Formula C₁₀H₁₉NO₃
badge Registry Numbers
MDL Number MFCD20278358
thermostat Physical Properties
Boiling Point 282.5±33.0 °C at 760 mmHg
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 bioactive molecules. It features a Boc-protected amine and a free hydroxyl group, allowing selective reactions in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing stereochemically defined pyrrolidine-based scaffolds, which are found in drugs targeting neurological disorders and viral infections. Also utilized in asymmetric synthesis to introduce specific stereocenters due to its rigid cyclic structure and defined stereochemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,200.00
inventory 250mg
10-20 days ฿4,800.00
inventory 1g
10-20 days ฿11,200.00
inventory 5g
10-20 days ฿35,560.00
inventory 500mg
10-20 days ฿7,680.00
(2S,4S)-tert-Butyl 4-hydroxy-2-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 bioactive molecules. It features a Boc-protected amine and a free hydroxyl group, allowing selective reactions in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing stereochemically defined pyrrolidine-based scaffolds, which are found in drugs targeting neurological disorders and viral infections. Also utilized in asymmetric synthesis t

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. It features a Boc-protected amine and a free hydroxyl group, allowing selective reactions in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing stereochemically defined pyrrolidine-based scaffolds, which are found in drugs targeting neurological disorders and viral infections. Also utilized in asymmetric synthesis to introduce specific stereocenters due to its rigid cyclic structure and defined stereochemistry.

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