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RARECHEM AH PB 0251 1676-86-4 C15H18N2O5
N6-Carbobenzoxy-L-lysine N-Carboxyanhydride Basic information |
Product Name: | N6-Carbobenzoxy-L-lysine N-Carboxyanhydride |
Synonyms: | N6-Carbobenzoxy-L-lysine N-Carboxyanhydride;(S)-[4-(2,5-Dioxo-4-oxazolidinyl)butyl]carbaMic Acid Phen;L-[4-(2,5-Dioxo-4-oxazolidinyl)butyl]carbaMic Acid Benzyl Ester;Lys(Z)-NCA;N-[(4S)-4-(2,5-Dioxo-4-oxazolidinyl)butyl]carbaMic Acid PhenylMethyl Ester;CarbaMic acid, [4-(2,5-dioxo-4-oxazolidinyl)butyl]-, phenylMethyl ester,(S)-;L-N-Benzoyloxycarbonyl lysine n-carboxyanhydride |
CAS: | 1676-86-4 |
MF: | C15H18N2O5 |
MW: | 306.31382 |
EINECS: | |
Product Categories: | Amino Acids & Derivatives;Aromatics;Chiral Reagents;Heterocycles |
Mol File: | 1676-86-4.mol |
N6-Carbobenzoxy-L-lysine N-Carboxyanhydride Chemical Properties |
Safety Information |
N6-Carbobenzoxy-L-lysine N-Carboxyanhydride Usage And Synthesis |
Usage | 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 infect ed 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 infect ion of tomato cuttings by F. lycopersici but was also toxic to the plants. Polyglutamic acid had no effect on the fungi in vitro. |
N6-Carbobenzoxy-L-lysine N-Carboxyanhydride Preparation Products And Raw |
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