N-6-Trifluoroacetyl-L-lysine

Base Information

  • PRODUCT:N-6-Trifluoroacetyl-L-lysine
  • CAS.:10009-20-8
  • MF:C8H13F3N2O3
  • Molecular Weight:242.198
  • Purity:99%

Product Details

CAS: 10009-20-8

MF: C8H13F3N2O3

Quality Factory Hot Selling N-6-Trifluoroacetyl-L-lysine 10009-20-8 with Fast Shipping

  • Molecular Formula:C8H13F3N2O3
  • Molecular Weight:242.198
  • Vapor Pressure:6.55E-07mmHg at 25°C 
  • Melting Point:258 °C 
  • Refractive Index:1.444 
  • Boiling Point:382.5 °C at 760 mmHg 
  • PKA:2.51±0.24(Predicted) 
  • Flash Point:185.1 °C 
  • PSA:92.42000 
  • Density:1.333 g/cm3 
  • LogP:1.33830 

N-6-Trifluoroacetyl-L-lysine(Cas 10009-20-8) Usage

Definition

ChEBI: An N6-acyl-L-lysine where the N6-acyl group is trifluoroacetyl.

Description N6-Trifluoroacetyl-L-lysine is a derivative of lysine that is used in peptide synthesis. It protects lysine from oxidation during peptide synthesis and helps form bonds between amino acids.
Uses N-6-Trifluoroacetyl-L-lysine N-carboxyanhydride is used to form bonds between amino acids and protect lysine from oxidation during peptide synthesis.

InChI:InChI=1/C8H13F3N2O3/c9-8(10,11)7(16)13-4-2-1-3-5(12)6(14)15/h5H,1-4,12H2,(H,13,16)(H,14,15)/t5-/m0/s1

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10009-20-8 Relevant articles

Genetically Encoded Libraries of Nonstandard Peptides

Takashi Kawakami, Hiroshi Murakami

, Journal of Nucleic Acids, 14 October 2012

Each enantiomer of N-chloroacetyltyrosine was reassigned to the initiation AUG codon. (c)Selection of cyclic peptides containing N-6-trifluoroacetyl-L lysine against sirtuin 2 (SIRT2). Each enantiomer of N-chloroacetyl-tyrosine was reassigned to the initiation AUG codon and N-6-trifluoroacetyl-L-lysine ( CF3K) was reassigned to the elongation AUG codon.

Control of lysyl oxidase activity through site-specific deuteration of lysine

Pestov, Nikolay B.,Okkelman, Irina A.,Shmanai, Vadim V.,Hurski, Alaksiej L.,Giaccia, Amato J.,Shchepinov, Mikhail S.

, p. 255 - 258 (2011)

Lysyl oxidase (LOX) is implicated in sev...

THERAPIES FOR CANCER USING ISOTOPICALLY SUBSTITUTED LYSINE

-

Page/Page column 7, (2009/10/22)

Methods of treatment and substances for ...

Polypeptides. XIV. The synthesis of some oligopeptides containing lysine and glutamic acid residues.

Moore,Rydon,Smithers

, p. 2349 - 2359 (2007/10/06)

-

10009-20-8 Process route

S-ethyl trifluoroacetate
383-64-2

S-ethyl trifluoroacetate

L-Lysine hydrochloride
657-27-2,10098-89-2,26124-78-7

L-Lysine hydrochloride

(S)-6-trifluoroacetylamino-2-aminohexanoic acid
10009-20-8,96193-68-9

(S)-6-trifluoroacetylamino-2-aminohexanoic acid

Conditions
Conditions Yield
With sodium hydroxide;
 
ethyl trifluoroacetate,
383-63-1

ethyl trifluoroacetate,

L-Lysine hydrochloride
657-27-2,10098-89-2,26124-78-7

L-Lysine hydrochloride

(S)-6-trifluoroacetylamino-2-aminohexanoic acid
10009-20-8,96193-68-9

(S)-6-trifluoroacetylamino-2-aminohexanoic acid

Conditions
Conditions Yield
With sodium; In ethanol; at 5 - 20 ℃;
62%
L-Lysine hydrochloride; With ethanol; sodium;
ethyl trifluoroacetate,; In ethanol; at 20 ℃; Cooling with ice;
With acetic acid; In ethanol;
62%
L-Lysine hydrochloride; With sodium; In ethanol; for 1h;
ethyl trifluoroacetate,; at 5 - 20 ℃; for 3h;
With acetic acid; for 0.166667h;
56%

10009-20-8 Upstream products

  • 383-64-2
    383-64-2

    S-ethyl trifluoroacetate

  • 657-27-2
    657-27-2

    L-Lysine hydrochloride

  • 383-63-1
    383-63-1

    ethyl trifluoroacetate,

  • 16079-52-0
    16079-52-0

    sodium salt of L-lysine

10009-20-8 Downstream products

  • 14905-30-7
    14905-30-7

    (2S)-2-{[(benzyloxy)carbonyl]amino}-6-[(trifluoroacetyl)amino]hexanoic acid

  • 42267-27-6
    42267-27-6

    Nε-trifluoroacetyl-L-lysine Nα-carboxanhydride

  • 112139-30-7
    112139-30-7

    C9H11Cl2F3N2O3

  • 41918-63-2
    41918-63-2

    Nα-(o-nitrophenylsulfenyl)-Nε-(trifluoroacetyl)lysine

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