Most efficient reagent for the selective preparation of N - (9-fluorenylmethoxycarbonyl) derivatives of hydroxy-amino acids in high yield. Dipeptide formation is lower than with the chloroformate, Fmoc-Cl. It has been employed in the synthesis of glycopeptides.

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The fluorenylmethoxycarbonyl protecting group (Fmoc) is a base-labile amine protecting group used in organic synthesis, particularly in peptide synthesis. [1] It is popular for its stability toward acids and hydrolysis and its selective removal by weak bases, such as piperidine , without affecting most other protecting groups or sensitive ...

Fmoc-OSu;9-Fluorenylmethyl succinimidyl carbonate;1-(9H-Fluorenylmethoxycarbonyloxy)2,5-pyrrolidinedione

Fmoc-OSu; Documents: SDS | Specifications | C of A & Other Certificates | Analytical Charts. Size Unit Price Philadelphia, PA Portland, OR Japan* Quantity; 5G: $51.00. 3 : 1 : ≥100 : 25G: $152.00. 6 : 4 : ≥100 : Added to Your Shopping Cart. Add to cart. Request Quote * Items in stock locally ship in 1-2 business days. Items from Japan stock ...

Fmoc-OSu is most commonly used nowadays due to the increased stability of this succinimide carbonate. It also has lower unproductive formation of oligopeptides that can occur during preparation of Fmoc amino acid derivatives. Additional …

ChemSpider record containing structure, synonyms, properties, vendors and database links for Fmoc-Osu, 82911-69-1, WMSUFWLPZLCIHP-UHFFFAOYSA-N

Fmoc-Succinimide: A succinimidyl carbonate group for peptide synthesis. CAS Number: 82911-69-1. Synonyms: N- (9-Fluorenylmethoxycarbonyloxy)succinimide, Fmoc-OSu. Purity: ≥98%.

Sequence-defined positioning of amine and amide residues to control catechol driven wet adhesion: This study uses Fmoc-OSu for selective functionalization of amines, demonstrating its role in synthesizing complex molecules with specific adhesive properties (Fischer et al., 2020).

Oct 15, 2002 · Alternate Name: Fmoc-OSu. Physical Data: mp 151 °C. Solubility: soluble in organic solvents such THF, dioxane, DMF, CH 2 Cl 2 as well as alcohols. Please see also the section on Fmoc-Cl in this encyclopedia; Fmoc-OSu undergoes many of the same reactions as Fmoc-Cl, but at a somewhat slower rate than Fmoc-Cl. Form Supplied in: white solid.