(S)-2-(Aminomethyl)-1-Boc-pyrrolidine

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Reagent Code: #66358
label
Alias S-tert-butoxycarbonyl-2-(aminoethyl)pyrrolidine
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CAS Number 119020-01-8

science Other reagents with same CAS 119020-01-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.28 g/mol
Formula C₁₀H₂₀N₂O₂
badge Registry Numbers
MDL Number MFCD03419257
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

This chemical is widely used as a chiral building block in the synthesis of pharmaceutical compounds, particularly in the production of active pharmaceutical ingredients (APIs) that require specific stereochemistry. Its Boc-protected amino group allows for selective deprotection, making it a valuable intermediate in multi-step organic synthesis. It is often employed in the development of drugs targeting neurological disorders, cardiovascular diseases, and other therapeutic areas where enantiomeric purity is critical. Additionally, it serves as a precursor in the synthesis of peptidomimetics and other biologically active molecules, enhancing their stability and bioavailability. Its versatility and compatibility with various synthetic methodologies make it a key component in medicinal chemistry research and drug development.

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Test Parameter Specification
Appearance Colorless to almost colorless clear liquid
Purity 96.5-100
Specific rotation [α]20/D (c=1, CHCl3) -50.0 to -46.0
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿420.00
inventory 5g
10-20 days ฿5,320.00
inventory 1g
10-20 days ฿1,160.00

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(S)-2-(Aminomethyl)-1-Boc-pyrrolidine
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This chemical is widely used as a chiral building block in the synthesis of pharmaceutical compounds, particularly in the production of active pharmaceutical ingredients (APIs) that require specific stereochemistry. Its Boc-protected amino group allows for selective deprotection, making it a valuable intermediate in multi-step organic synthesis. It is often employed in the development of drugs targeting neurological disorders, cardiovascular diseases, and other therapeutic areas where enantiomeric purity is critical. Additionally, it serves as a precursor in the synthesis of peptidomimetics and other biologically active molecules, enhancing their stability and bioavailability. Its versatility and compatibility with various synthetic methodologies make it a key component in medicinal chemistry research and drug development.
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