(R)-Benzyl 2-(hydroxymethyl)pyrrolidine-1-carboxylate

96%

Reagent Code: #230290
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CAS Number 72597-18-3

science Other reagents with same CAS 72597-18-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.28 g/mol
Formula C₁₃H₁₇NO₃
badge Registry Numbers
MDL Number MFCD02683223
thermostat Physical Properties
Boiling Point 382°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.135 g/mL at 25 °C
Storage 2-8℃

description Product Description

Used in pharmaceutical synthesis as a chiral building block for the development of bioactive molecules. Its pyrrolidine core with a hydroxymethyl group enables functionalization for drug design, particularly in creating enzyme inhibitors or receptor ligands. The compound's stereochemistry makes it valuable in asymmetric synthesis, where high enantiomeric purity is required. Commonly employed in the preparation of protease inhibitors and central nervous system agents. Also utilized in the development of novel therapeutics where nitrogen-containing heterocycles are key structural elements.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿269.50
5g
10-20 days ฿1,840.00
(R)-Benzyl 2-(hydroxymethyl)pyrrolidine-1-carboxylate
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Used in pharmaceutical synthesis as a chiral building block for the development of bioactive molecules. Its pyrrolidine core with a hydroxymethyl group enables functionalization for drug design, particularly in creating enzyme inhibitors or receptor ligands. The compound's stereochemistry makes it valuable in asymmetric synthesis, where high enantiomeric purity is required. Commonly employed in the preparation of protease inhibitors and central nervous system agents. Also utilized in the development of n

Used in pharmaceutical synthesis as a chiral building block for the development of bioactive molecules. Its pyrrolidine core with a hydroxymethyl group enables functionalization for drug design, particularly in creating enzyme inhibitors or receptor ligands. The compound's stereochemistry makes it valuable in asymmetric synthesis, where high enantiomeric purity is required. Commonly employed in the preparation of protease inhibitors and central nervous system agents. Also utilized in the development of novel therapeutics where nitrogen-containing heterocycles are key structural elements.

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