(S)-1-Fmoc-3-Pyrrolidinol

≥97%

Reagent Code: #235201
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CAS Number 215178-38-4

science Other reagents with same CAS 215178-38-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 309.36 g/mol
Formula C₁₉H₁₉NO₃
thermostat Physical Properties
Melting Point 106-110ºC
Boiling Point 496.1ºC
inventory_2 Storage & Handling
Density 1.295g/cm3
Storage Room temperature, dry

description Product Description

Used in peptide synthesis and medicinal chemistry as a chiral building block for developing bioactive molecules. Its hydroxyl and amine protecting groups allow selective reactions, making it valuable in constructing complex organic compounds, particularly in pharmaceuticals targeting neurological and psychiatric disorders. Commonly employed in solid-phase synthesis due to compatibility with Fmoc-strategy. Also utilized in the preparation of enzyme inhibitors and receptor ligands where stereochemistry plays a critical role in biological activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,250.00
inventory 1g
10-20 days ฿3,770.00
inventory 5g
10-20 days ฿16,330.00
(S)-1-Fmoc-3-Pyrrolidinol
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Used in peptide synthesis and medicinal chemistry as a chiral building block for developing bioactive molecules. Its hydroxyl and amine protecting groups allow selective reactions, making it valuable in constructing complex organic compounds, particularly in pharmaceuticals targeting neurological and psychiatric disorders. Commonly employed in solid-phase synthesis due to compatibility with Fmoc-strategy. Also utilized in the preparation of enzyme inhibitors and receptor ligands where stereochemistry pla

Used in peptide synthesis and medicinal chemistry as a chiral building block for developing bioactive molecules. Its hydroxyl and amine protecting groups allow selective reactions, making it valuable in constructing complex organic compounds, particularly in pharmaceuticals targeting neurological and psychiatric disorders. Commonly employed in solid-phase synthesis due to compatibility with Fmoc-strategy. Also utilized in the preparation of enzyme inhibitors and receptor ligands where stereochemistry plays a critical role in biological activity.

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