(R)-1-Cbz-3-(hydroxymethyl)pyrrolidine

97%

Reagent Code: #230834
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CAS Number 192214-05-4

science Other reagents with same CAS 192214-05-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.28 g/mol
Formula C₁₃H₁₇NO₃
badge Registry Numbers
MDL Number MFCD06410562
thermostat Physical Properties
Boiling Point 382 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in pharmaceutical synthesis as a chiral building block, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its hydroxymethyl and amine functionalities allow for further chemical modifications, making it valuable in constructing complex molecules. Commonly employed in the preparation of protease inhibitors and other bioactive compounds where a pyrrolidine scaffold enhances metabolic stability and target binding. The Cbz-protected amine ensures selective reactivity during multi-step syntheses, especially in peptide-related chemistry and heterocyclic drug candidates.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿2,500.00
250mg
10-20 days ฿3,390.00
1g
10-20 days ฿4,530.00
5g
10-20 days ฿14,760.00
10g
10-20 days ฿29,520.00
(R)-1-Cbz-3-(hydroxymethyl)pyrrolidine
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Used in pharmaceutical synthesis as a chiral building block, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its hydroxymethyl and amine functionalities allow for further chemical modifications, making it valuable in constructing complex molecules. Commonly employed in the preparation of protease inhibitors and other bioactive compounds where a pyrrolidine scaffold enhances metabolic stability and target binding. The Cbz-protected amine ensure

Used in pharmaceutical synthesis as a chiral building block, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its hydroxymethyl and amine functionalities allow for further chemical modifications, making it valuable in constructing complex molecules. Commonly employed in the preparation of protease inhibitors and other bioactive compounds where a pyrrolidine scaffold enhances metabolic stability and target binding. The Cbz-protected amine ensures selective reactivity during multi-step syntheses, especially in peptide-related chemistry and heterocyclic drug candidates.

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