10009-20-8

  • Product NameN-6-Trifluoroacetyl-L-lysine
  • Molecular FormulaC8H13F3N2O3
  • Molecular Weight242.198
  • Purity99%
Inquiry

Product Details

Quick Details

  • CasNo: 10009-20-8
  • Molecular Formula: C8H13F3N2O3
  • Purity: 99%

N-6-Trifluoroacetyl-L-lysine 10009-20-8 Good Price In Medicine

  • 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

Chemical Properties

Off-White Solid

Uses

N(6)-trifluoroacetyl-L-lysine is an N(6)-acyl-L-lysine where the N(6)-acyl group is trifluoroacetyl. Used in the synthesis of new arborescent architectures of poly(L-lysine), called lysine dendrigraft (DGL) polymers. The amino acid N 6 -trifluoroacetyl-l-lysine is similar to TMSK but designed for the detection of the CF 3 group by 19 F NMR spectroscopy.

Definition

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

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

10009-20-8 Relevant articles

Selective Detection of Folic Acid Using a Water-Stable Fluorescent CsPbBr3/Cs4PbBr6 Perovskite Nanocrystal Probe

Wen-Zhi She,Rui-Xian Zhao,Jin-Zhou Liu,Hai-Chi Zhang,Rong Sheng Li,Meng-Ting Liu,Chuan-Hua Zhou *,Jian Ling *ORCID andQiue Cao

Chemosensors 2023, 11(1), 19;

In this work, we improved the reported aqueous emulsion method for the synthesis of water-stable cesium lead bromide PNCs using CsBr, PbBr2, N-6-trifluoroacetyl-l-lysine, and oleylamine (OLA) as the raw materials.

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...

Sweet boron: boron-containing sugar derivatives as potential agents for boron neutron capture therapy

D Imperio, L Panza

Symmetry 2022, 14(2), 182;

The polymer was obtained by reaction of MeOPegNH 2 with N6-trifluoroacetyl-l-lysine N-carboxyanhydride, followed by deprotection of the ω-amino groups and their functionalization …

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

  • 41918-63-2
    41918-63-2

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

  • 42267-27-6
    42267-27-6

    Nε-trifluoroacetyl-L-lysine Nα-carboxanhydride

  • 103300-89-6
    103300-89-6

    Nε-(trifluoroacetyl)-L-lysyl-L-proline

;

Relevant Products