1-Boc-3-Isopropylamino-pyrrolidine

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Reagent Code: #152459
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CAS Number 1289385-05-2

science Other reagents with same CAS 1289385-05-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.331 g/mol
Formula C₁₂H₂₄N₂O₂
badge Registry Numbers
MDL Number MFCD09953083
thermostat Physical Properties
Boiling Point 299.0±33.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.00 g/cm3
Storage 2-8°C

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) requiring pyrrolidine-based scaffolds. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of bioactive molecules, including central nervous system agents and enzyme inhibitors. The Boc-protected structure enhances stability during reactions and enables controlled deprotection under mild acidic conditions, making it valuable in peptide and heterocyclic chemistry. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its chiral and sterically defined framework.

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inventory 1g
10-20 days ฿41,400.00

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1-Boc-3-Isopropylamino-pyrrolidine
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) requiring pyrrolidine-based scaffolds. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of bioactive molecules, including central nervous system agents and enzyme inhibitors. The Boc-protected structure enhances stability during reactions and enables controlled deprotection under mild acidic condition

Used as an intermediate in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) requiring pyrrolidine-based scaffolds. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of bioactive molecules, including central nervous system agents and enzyme inhibitors. The Boc-protected structure enhances stability during reactions and enables controlled deprotection under mild acidic conditions, making it valuable in peptide and heterocyclic chemistry. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its chiral and sterically defined framework.

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