N6-Carbobenzoxy-L-lysine N-Carboxyanhydride

CAS : 1676-86-4

Ref. TR-C175990

Informations sur le produit

• Nom: N6-Carbobenzoxy-L-lysine N-Carboxyanhydride
• Synonymes: Carbamic acid, N-[(4S)-4-(2,5-dioxo-4-oxazolidinyl)butyl]-, phenylmethyl ester, Carbamic acid, [4-(2,5-dioxo-4-oxazolidinyl)butyl]-, benzyl ester, L- (8CI), Carbamic acid, [4-(2,5-dioxo-4-oxazolidinyl)butyl]-, phenylmethyl ester, (S)- (9CI), N-e-Benzyloxycarbonyl-L-lysine-N-carboxyanhydride, N6-Benzyloxycarbonyl-L-lysine N-carboxyanhydride, N6-Carbobenzyloxy-L-lysine N-carboxyanhydride, NCA-N-e-benzyloxycarbonyl-L-lysine, Ne-Benzyloxycarbonyl-L-lysine N-carboxyanhydride, Ne-Benzyloxycarbonyl-L-lysine carboxyanhydride, Ne-Carbobenzoxylysine N-carboxy anhydride, Ne-Cbz-L-Lysine Na-carboxyanhydride, Z-L-Lysine N-carboxyanhydride, e-Benzyloxycarbonyl-L-lysine N-carboxyanhydride

Description

Applications A L-lysine derivative used in the preparation of Polylysine, a synthetic, basic poly-α-amino acid. Polylysine inhibited fungal penetration and polyphenol formation in susceptible sweet potatoes infected with C. fimbriata and caused some inhibition of fungal growth, a lessening of the penetration by the fungus, and more callus formation in resistant sweet potatoes. The compound inhibited the infection of tomato cuttings by F. lycopersici but was also toxic to the plants. Polyglutamic acid had no effect on the fungi in vitro.
References Buchanan-Davidson, D.J., et al.: Science, 132, 1664 (1960),

• Marque: TRC

Propriétés chimiques

• Masse moléculaire: 306.31
• Formule: C₁₅H₁₈N₂O₅
• Couleur/Forme: Neat
• InChI: InChI=1S/C15H18N2O5/c18-13-12(17-15(20)22-13)8-4-5-9-16-14(19)21-10-11-6-2-1-3-7-11/h1-3,6-7,12H,4-5,8-10H2,(H,16,19)(H,17,20)/t12-/m0/s1
• Code InChI: InChIKey=HLLIDIRDRPSCHN-LBPRGKRZSA-N
• SMILES: O=C(NCCCC[C@@H]1NC(=O)OC1=O)OCc1ccccc1