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Home > Encyclopedia > N6-Trifluoroacetyl-L-lysine N-Carboxyanhydride

N6-Trifluoroacetyl-L-lysine N-Carboxyanhydride

N6-Trifluoroacetyl-L-lysine N-Carboxyanhydride structure

N6-Trifluoroacetyl-L-lysine N-Carboxyanhydride 

structure
  • CAS No:

    42267-27-6

  • Formula:

    C9H11F3N2O4

  • Chemical Name:

    N6-Trifluoroacetyl-L-lysine N-Carboxyanhydride

  • Synonyms:

    N-[4-[(4S)-2,5-dioxooxazolidin-4-yl]butyl]-2,2,2-trifluoro-acetamide;e-Trifluoroacetyl-Lysine, NCA;N-Trifluoroacetyl-L-lysine N-carboxyanhydride;N-(4-(2,5-Dioxo-4-oxazolidinyl)butyl)-2,2,2-trifluoroacetamide;N6-Trifluoroacetyl-L-lysine N-Carboxyanhydride;L-Lysine-N-Trifluoroacetyl-N-Carboxyanhydride;(S)-N-[4-(2,5-Dioxo-4-oxazolidinyl)butyl]-2,2,2-trifluoroacetaMide;N-[4-[(4S)-2,5-Dioxo-4-oxazolidinyl]butyl]-2,2,2-trifluoroacetaMide

  • Categories:

    Pharmaceutical Intermediates  >  Bulk Drug Intermediates

Description

N6-Trifluoroacetyl-L-lysine N-Carboxyanhydride is a N6-trifluoroacetylated lysine derivative that is used in the synthesis of peptides. It is a racemic mixture of L and D forms, which is hydrolyzed to form L-glutamic acid, NH4Cl, and CO2. N6-Trifluoroacetyl-L-lysine N-Carboxyanhydride has been shown to be useful in the formation of bonds between amino acids, such as lysine and dipeptides. The compound is also used for the protection of lysine against oxidation during peptide synthesis.


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N6-Trifluoroacetyl-L-lysine N-Carboxyanhydride Basic Attributes

268.19

268.19

610-008-1

White to Off-White

2933.79.8500

Characteristics

1.377

92-93℃ (DEC.)

9.27±0.40(Predicted)

Inert atmosphere,Store in freezer, under -20°C

N6-Trifluoroacetyl-L-lysine N-Carboxyanhydride Use and Manufacturing

Used in the synthesis of new arborescent architectures of poly(L-lysine), called lysine dendrigraft (DGL) polymers. DGL polymers were prepd. through a multiple-generation scheme (up to generation 5) in a weakly acidic aq. medium by polycondensing N.vepsiln.-trifluoroacetyl-L-lysine-N-carboxyanhydride (Lys(Tfa)-NCA) onto the previous generation G(n-1) of DGL, which was used as a macroinitiator.


L-Lys(Tfa)-NCA (N6-Trifluoroacetyl-L-lysine N-Carboxyanhydride) can be used in the synthesis of new arborescent architectures of poly(L-lysine), called lysine dendrigraft (DGL) polymers.

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