96840

H-Lys(Z)-OH

≥99.0% (NT), for peptide synthesis

• Synonym(e): N_ε-Z-L-lysin, N⁶-Carbobenzyloxy-L-lysin
• Lineare Formel: C₆H₅CH₂OOCNH(CH₂)₄CH(NH₂)COOH
• CAS-Nummer: 1155-64-2
• Molekulargewicht: 280.32
• Beilstein: 2222482
• EG-Nummer: 214-585-7
• MDL-Nummer: MFCD00002638
• UNSPSC-Code: 12352209
• eCl@ss: 32160406
• PubChem Substanz-ID: 57653788
• NACRES: NA.22

Eigenschaften

• product name: H-Lys(Z)-OH, ≥99.0% (NT)
• Assay: ≥99.0% (NT)
• Form: powder
• Optische Aktivität: [α]20/D +15.5±1°, c = 1% in 1 M HCl
• Eignung der Reaktion: reaction type: solution phase peptide synthesis
• mp (Schmelzpunkt): 259 °C (dec.) (lit.)
• Anwendung(en): peptide synthesis
• SMILES String: N[C@@H](CCCCNC(=O)OCc1ccccc1)C(O)=O
• InChI: 1S/C14H20N2O4/c15-12(13(17)18)8-4-5-9-16-14(19)20-10-11-6-2-1-3-7-11/h1-3,6-7,12H,4-5,8-10,15H2,(H,16,19)(H,17,18)/t12-/m0/s1
• InChIKey: CKGCFBNYQJDIGS-LBPRGKRZSA-N

Beschreibung

Allgemeine Beschreibung

H-Lys(Z)-OH also known as N6-carbobenzyloxy-L-lysine, commonly used as a reagent in the synthesis of peptides.

Anwendung

H-Lys(Z)-OH serves as a reactant for the synthesis of various peptides such as boc-Glu(OBzl)-Lys(Z)-OH and tert-butyl-6-(((benzyloxy)carbonyl)amino)-2-bromohexanoate. Additionally, it is used in the Fuchs-Farthing method to synthesize lysine NCA, which is a block copolymer.

Sicherheitshinweise

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