47624

Fmoc-Lys(Boc)-OH

≥98.0% (HPLC), for peptide synthesis

• Synonym(e): N_α-Fmoc-N_ε-Boc-L-lysin
• Empirische Formel (Hill-System): C₂₆H₃₂N₂O₆
• CAS-Nummer: 71989-26-9
• Molekulargewicht: 468.54
• Beilstein: 4217767
• EG-Nummer: 276-256-4
• MDL-Nummer: MFCD00037138
• UNSPSC-Code: 12352209
• eCl@ss: 32160406
• PubChem Substanz-ID: 57651044
• NACRES: NA.26

Eigenschaften

• Produktbezeichnung: Fmoc-Lys(Boc)-OH, ≥98.0% (HPLC)
• Assay: ≥98.0% (HPLC)
• Form: solid
• Optische Aktivität: [α]20/D −12±1°, c = 1% in DMF
• Eignung der Reaktion: reaction type: Fmoc solid-phase peptide synthesis
• Anwendung(en): peptide synthesis
• Funktionelle Gruppe: Boc; Fmoc
• Lagertemp.: 2-8°C
• SMILES String: CC(C)(C)OC(=O)NCCCC[C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O
• InChI: 1S/C26H32N2O6/c1-26(2,3)34-24(31)27-15-9-8-14-22(23(29)30)28-25(32)33-16-21-19-12-6-4-10-17(19)18-11-5-7-13-20(18)21/h4-7,10-13,21-22H,8-9,14-16H2,1-3H3,(H,27,31)(H,28,32)(H,29,30)/t22-/m0/s1
• InChIKey: UMRUUWFGLGNQLI-QFIPXVFZSA-N

Beschreibung

Allgemeine Beschreibung

Fmoc-Lys(Boc)-OH is an amino acid derivative used as a reagent in Fmoc solid-phase peptide synthesis.

Anwendung

Fmoc-Lys(Boc)-OH can be used for:

• The solid-phase synthesis of pentasubstituted dihydroimidazolylbutyl dihydroimidazol-3-ium salts by coupling with p-methylbenzhydrylamine (MBHA) resin.
• Fmoc-based peptide synthesis of bis-naphthalene diimide, a threading intercalator.
• Synthesis of ε-Boc-ε-(3,5-bis-trifluoromethyl-benzyl)-α-Fmoc-L-Lysine to be used as ¹⁹F NMR based screening tool.

Sicherheitshinweise

• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable
• Persönliche Schutzausrüstung: Eyeshields, Gloves, type N95 (US)