(S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-oxopiperidine-2-carboxylicacid

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Reagent Code: #237865
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CAS Number 1221793-43-6

science Other reagents with same CAS 1221793-43-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 365.38 g/mol
Formula C₂₁H₁₉NO₅
badge Registry Numbers
MDL Number MFCD03094868
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its structure allows for selective functionalization in peptide-like chains, making it valuable in medicinal chemistry for building complex, chiral molecules. Commonly employed in solid-phase peptide synthesis due to the Fmoc group, which provides orthogonal protection for amine functionalities. The ketone group enables further derivatization, such as reductive amination or nucleophilic addition, facilitating the creation of diverse compound libraries for drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,230.00
inventory 250mg
10-20 days ฿8,820.00
inventory 1g
10-20 days ฿25,410.00

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(S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-oxopiperidine-2-carboxylicacid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its structure allows for selective functionalization in peptide-like chains, making it valuable in medicinal chemistry for building complex, chiral molecules. Commonly employed in solid-phase peptide synthesis due to the Fmoc group, which provides orthogonal protection for amine functionalities. The ketone group enables further derivatiza

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its structure allows for selective functionalization in peptide-like chains, making it valuable in medicinal chemistry for building complex, chiral molecules. Commonly employed in solid-phase peptide synthesis due to the Fmoc group, which provides orthogonal protection for amine functionalities. The ketone group enables further derivatization, such as reductive amination or nucleophilic addition, facilitating the creation of diverse compound libraries for drug discovery.

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