N2-(Benzyloxycarbonyl)-N6-(tert-butoxycarbonyl)-L-lysine

CAS : 2389-60-8

Ref. 3D-FB47732

Informations sur le produit

• Nom: N2-(Benzyloxycarbonyl)-N6-(tert-butoxycarbonyl)-L-lysine
• Synonymes: Z-Lys(Boc)-OHN- a- benzyloxycarbonyl- N- epsilon- Boc- L- lysine (2S) - 2- {[(benzyloxy) carbonyl] amino} - 6- [(tert- butoxycarbonyl) amino] hexanoic acid, (2S)-6-[(2-Methylpropan-2-yl)oxycarbonylamino]-2-(phenylmethoxycarbonylamino)hexanoic acid, (S)-2-(Benzyloxycarbonylamino)-6-(tert-butoxycarbonylamino)hexanoic acid, <span class="text-smallcaps">L</span>-Lysine, N⁶-[(1,1-dimethylethoxy)carbonyl]-N²-[(phenylmethoxy)carbonyl]-, Benzyloxycarbonylbutoxycarbonyllysine, Boc-D-Phg-OH~N-(tert-Butoxycarbonyl)-D-phenylglycine, Butoxycarbonylcarbobenzoxylysine, Cbz-<span class="text-smallcaps">L</span>-Lys(Boc)-OH, Cbz-D-Lys(Boc)-OH, Cbz-Lys(Boc)-OH, Lysine, N²,N⁶-dicarboxy-, N²-benzyl N⁶-tert-butyl ester, <span class="text-smallcaps">L</span>-, N(alpha)-Z-N(epsilon)-boc-D-lysine, N-a-CBZ-(N-e-BOC)-L-Lys, N-benzyloxycarbonyl-n'-(tert-butoxycarbonyl)-l-lysine, N-α-Benzyloxycarbonyl-N-ε-tert-butoxycarbonyl-<span class="text-smallcaps">L</span>-lysine, N2-Benzyloxycarbonyl-N6-tert-butoxycarbonyl-D-lysine, N²-Benzyloxycarbonyl-N⁶-tert-butoxycarbonyl-<span class="text-smallcaps">L</span>-lysine, N⁶-[(1,1-Dimethylethoxy)carbonyl]-N²-[(phenylmethoxy)carbonyl]-<span class="text-smallcaps">L</span>-lysine, N^ε-[(tert-Butoxy)carbonyl]-N^α--[(benzyloxy)carbonyl]-<span class="text-smallcaps">L</span>-lysine, NSC 164047, N~2~-[(benzyloxy)carbonyl]-N~6~-(tert-butoxycarbonyl)-D-lysine, N~2~-[(benzyloxy)carbonyl]-N~6~-(tert-butoxycarbonyl)-L-lysine, N~2~-[(benzyloxy)carbonyl]-N~6~-(tert-butoxycarbonyl)lysine, Z-D-Lys(Boc)-OH, Z-D-Lys(Boc)-OH (cryst.), Z-Lys(Boc)-OH, n^(epsilum)-(tert-Butoxycarbonyl)-N^(alpha)-carbobenzoxy-L-lysine, na-cbz-N-epsilon-T-boc-D-lysine
• CAS: 2389-60-8

Description

N2-(Benzyloxycarbonyl)-N6-(tert-butoxycarbonyl)-L-lysine is an amino acid that is used in the synthesis of peptides. The tert-butyl group on the nitrogen atom provides a site for acylation. This compound was synthesized by orthogonal protection of the lysine side chain with benzyl and tert-butyl groups.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 380.44 g/mol
• Formule: C₁₉H₂₈N₂O₆
• Degré de pureté: Min. 98 Area-%
• Couleur/Forme: Clear Liquid