(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-cyanophenyl)propanoic acid

96%

Reagent Code: #231452
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CAS Number 517905-92-9

science Other reagents with same CAS 517905-92-9

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inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used in peptide synthesis as a chiral building block for the preparation of enantiomerically pure compounds. Its structure allows for selective coupling reactions, making it valuable in the development of pharmaceutical intermediates, particularly in the synthesis of protease inhibitors and other bioactive molecules. The presence of the cyano group enables further functionalization, while the Fmoc group provides orthogonal protection for amine functionalities during solid-phase peptide synthesis. Commonly employed in research settings for constructing complex organic molecules requiring stereochemical control.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,100.00
inventory 250mg
10-20 days ฿6,400.00
inventory 1g
10-20 days ฿16,970.00

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(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-cyanophenyl)propanoic acid
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Used in peptide synthesis as a chiral building block for the preparation of enantiomerically pure compounds. Its structure allows for selective coupling reactions, making it valuable in the development of pharmaceutical intermediates, particularly in the synthesis of protease inhibitors and other bioactive molecules. The presence of the cyano group enables further functionalization, while the Fmoc group provides orthogonal protection for amine functionalities during solid-phase peptide synthesis. Commonl

Used in peptide synthesis as a chiral building block for the preparation of enantiomerically pure compounds. Its structure allows for selective coupling reactions, making it valuable in the development of pharmaceutical intermediates, particularly in the synthesis of protease inhibitors and other bioactive molecules. The presence of the cyano group enables further functionalization, while the Fmoc group provides orthogonal protection for amine functionalities during solid-phase peptide synthesis. Commonly employed in research settings for constructing complex organic molecules requiring stereochemical control.

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