1676-86-4

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;L-Lys(Cbz)-NCA
• CAS NO: 1676-86-4
• Molecular Formula: C₁₅H₁₈N₂O₅
• Molecular Weight: 306.31382
• Product Categories: Amino Acids & Derivatives;Aromatics;Chiral Reagents;Heterocycles
• Mol File: 1676-86-4.mol
• Article Data: 72

Chemical Properties

• Appearance: /
• Density: 1.248 g/cm³
• Storage Temp.: 2-8°C
• Solubility: Chloroform (Very Slightly, Sonicated), DMSO (Slightly), Methanol (Slightly)
• PKA: 9.31±0.40(Predicted)
• Stability: Hygroscopic
• CAS DataBase Reference: N6-Carbobenzoxy-L-lysine N-Carboxyanhydride(CAS DataBase Reference)
• NIST Chemistry Reference: N6-Carbobenzoxy-L-lysine N-Carboxyanhydride(1676-86-4)
• EPA Substance Registry System: N6-Carbobenzoxy-L-lysine N-Carboxyanhydride(1676-86-4)

Safety Data

• Hazardous Substances Data: 1676-86-4(Hazardous Substances Data)

Usage

Uses

Different sources of media describe the Uses of 1676-86-4 differently. You can refer to the following data:
1. Like a L-lysine derivative, N6-Carbobenzoxy-L-lysine N-Carboxyanhydride can be used in the preparation of Polylysine, a synthetic, basic poly-α-amino acid.
2. 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.

Upstream product

• 405-39-0 N,N'-di-[(phenylmethoxy)carbonyl]-L-lysine 
• 32315-10-9 bis(trichloromethyl) carbonate 
• 1155-64-2 N₆-[(benzyloxy)carbonyl]-L-lysine 
• 32302-83-3 N-ε-benzyloxycarbonyl lysine 
• 75-44-5 phosgene 
• 1387552-55-7 C₂₁H₂₄N₂O₆ 
• 116-16-5 1,1,1,3,3,3-hexachloro-propan-2-one 
• 501-53-1 benzyl chloroformate 
• 56-87-1 L-lysine 
• 657-27-2 L-Lysine hydrochloride 
• 503-38-8 trichloromethyl chloroformate 

Downstream Products

• 102495-95-4 N⁶-benzyloxycarbonyl-L-lysine hydrazide 
• 59515-43-4 N^ε-benzyloxycarbonyl-L-lysine ethyl ester hydrochloride 
• 59515-43-4 N⁶-benzyloxycarbonyl-DL-lysine ethyl ester; hydrochloride 
• 108-32-7 1,2-propylene cyclic carbonate 
• 55226-85-2 tetra-(N-carbobenzoxy-L-lysine) 

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