(2R,4S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-((tert-butoxycarbonyl)amino)pyrrolidine-2-carboxylicacid

96%

Reagent Code: #232026
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CAS Number 1820570-42-0

science Other reagents with same CAS 1820570-42-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 452.50 g/mol
Formula C₂₅H₂₈N₂O₆
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Widely used in peptide synthesis, this compound serves as a protected chiral building block for the construction of complex peptides and peptidomimetics. Its stereochemistry allows for precise control in forming specific peptide sequences, particularly in solid-phase synthesis. The Fmoc group enables reversible N-terminal protection, compatible with mild base deprotection, making it ideal for stepwise elongation in automated synthesizers. The Boc group on the secondary amine provides orthogonal protection, allowing selective deprotection in multi-step syntheses. Commonly employed in the preparation of pharmaceutical intermediates, especially in the development of protease inhibitors and other bioactive molecules where stereochemical integrity is critical. Its utility in combinatorial chemistry and drug discovery makes it a valuable reagent in medicinal chemistry research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,070.00
inventory 250mg
10-20 days ฿13,570.00
inventory 500mg
10-20 days ฿25,540.00
inventory 1g
10-20 days ฿42,950.00
(2R,4S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-((tert-butoxycarbonyl)amino)pyrrolidine-2-carboxylicacid
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Widely used in peptide synthesis, this compound serves as a protected chiral building block for the construction of complex peptides and peptidomimetics. Its stereochemistry allows for precise control in forming specific peptide sequences, particularly in solid-phase synthesis. The Fmoc group enables reversible N-terminal protection, compatible with mild base deprotection, making it ideal for stepwise elongation in automated synthesizers. The Boc group on the secondary amine provides orthogonal protectio

Widely used in peptide synthesis, this compound serves as a protected chiral building block for the construction of complex peptides and peptidomimetics. Its stereochemistry allows for precise control in forming specific peptide sequences, particularly in solid-phase synthesis. The Fmoc group enables reversible N-terminal protection, compatible with mild base deprotection, making it ideal for stepwise elongation in automated synthesizers. The Boc group on the secondary amine provides orthogonal protection, allowing selective deprotection in multi-step syntheses. Commonly employed in the preparation of pharmaceutical intermediates, especially in the development of protease inhibitors and other bioactive molecules where stereochemical integrity is critical. Its utility in combinatorial chemistry and drug discovery makes it a valuable reagent in medicinal chemistry research.

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