(R)-tert-Butyl(2-(pyrrolidin-2-yl)ethyl)carbamate

96%

Reagent Code: #232214
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CAS Number 720000-05-5

science Other reagents with same CAS 720000-05-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.31 g/mol
Formula C₁₁H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD06656825
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected amine and pyrrolidine functionalities make it valuable in the preparation of bioactive molecules, including neurologically active compounds and receptor ligands. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemical integrity and compatibility with peptide-like structures.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿54,800.00
(R)-tert-Butyl(2-(pyrrolidin-2-yl)ethyl)carbamate
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected amine and pyrrolidine functionalities make it valuable in the preparation of bioactive molecules, including neurologically active compounds and receptor ligands. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemical integrity and compatibility with pe

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected amine and pyrrolidine functionalities make it valuable in the preparation of bioactive molecules, including neurologically active compounds and receptor ligands. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemical integrity and compatibility with peptide-like structures.

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