(S)-2-(3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)propanamido)propanoic acid

97%

Reagent Code: #237026
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CAS Number 850324-83-3

science Other reagents with same CAS 850324-83-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 382.41 g/mol
Formula C₂₁H₂₂N₂O₅
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used primarily in peptide synthesis as a chiral building block, this compound enables the introduction of protected amino acid functionalities with stereochemical control. Its fluorenylmethyloxycarbonyl (Fmoc) group allows for mild base-labile protection, making it ideal for solid-phase peptide synthesis. The compound’s (S)-configuration ensures enantioselective incorporation into peptide chains, preserving structural integrity and biological activity in the final product. It is especially valuable in the preparation of complex peptides and peptidomimetics for pharmaceutical and biochemical research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,520.00
inventory 250mg
10-20 days ฿2,440.00
inventory 1g
10-20 days ฿7,180.00
inventory 5g
10-20 days ฿33,640.00
(S)-2-(3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)propanamido)propanoic acid
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Used primarily in peptide synthesis as a chiral building block, this compound enables the introduction of protected amino acid functionalities with stereochemical control. Its fluorenylmethyloxycarbonyl (Fmoc) group allows for mild base-labile protection, making it ideal for solid-phase peptide synthesis. The compound’s (S)-configuration ensures enantioselective incorporation into peptide chains, preserving structural integrity and biological activity in the final product. It is especially valuable in th

Used primarily in peptide synthesis as a chiral building block, this compound enables the introduction of protected amino acid functionalities with stereochemical control. Its fluorenylmethyloxycarbonyl (Fmoc) group allows for mild base-labile protection, making it ideal for solid-phase peptide synthesis. The compound’s (S)-configuration ensures enantioselective incorporation into peptide chains, preserving structural integrity and biological activity in the final product. It is especially valuable in the preparation of complex peptides and peptidomimetics for pharmaceutical and biochemical research.

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