WebN3-Lys(Fmoc)-OH: Alternate Names (s)-α-azido-ε-(Fmoc-amino)-hexanoic acid; Background Information: A useful tool for the synthesis of branched, side-chain modified and cyclic peptides by Fmoc SPPS. The azido group is completely stable to piperidine and TFA, but can be readily converted to an amine on the solid phase or in solution by ... WebH-Lys(Fmoc)-OH C21H24N2O4 CID 7010541 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, …

The Fmoc‐Lys(Fmoc)‐Asp hypergelator forms self‐assembled …

WebFmoc-Lys (Boc)-OH Novabiochem®. CAS 71989-26-9, molar mass 468.54 g/mol. Physicochemical Information. Melting Point. 123 - 130 °C. Safety Information according … WebFmoc-Lys (ivDde)-OH Novabiochem®. CAS 204777-78-6, molar mass 574.72 g/mol. Safety Information according to GHS. Storage class. 10 - 13 Other liquids and solids. WGK. WGK 3 highly hazardous to water. Storage and Shipping Information. Storage. toddler southern belle dresses

Fmoc-Lys(Ac)-OH C23H26N2O5 - PubChem

WebNalpha-Boc-Nepsilon-Fmoc-D-lysine. Catalog # ABK220. CAS : 115186-31-7. Formula: C 26 H 32 N 2 O 6. M.W.: 468.53. Boc-D-Lys (Fmoc)-OH is one of the D-lysine derivatives utilized in Boc-SPPS. The Fmoc protecting group on the side chain is stable in acidic conditions, but can be removed with bases such as piperidine or morpholine. WebAs indicated in Table 1, the N α-Fmoc-N ε-Boc-l-Lys residue couples efficiently across the matrix studied. Robust, DNA-compatible Boc removal conditions have been developed (43) and their adaptation (pH 9.5 sodium borate buffer, 80 °C, 48 h) is demonstrated during the deprotection of the DNA-decamer conjugate (see below). WebFmoc-Lys (Fmoc)-OH ≥98.0% (HPLC) Synonym (s): Nα,Nε-di-Fmoc-L-lysine Empirical Formula (Hill Notation): C36H34N2O6 CAS Number: 78081-87-5 Molecular Weight: … toddler southern t shirts