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ChemicalBook CAS DataBase List epsilon-dinitrophenyllysine
1094-76-4

epsilon-dinitrophenyllysine synthesis

3synthesis methods
L-Lysine, N6-(2,4-dinitrophenyl)-N2-[[1-methyl-2-(phenylsulfonyl)ethoxy]carbonyl]-

1202639-02-8
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Benzene,(1-propen-1-ylsulfonyl)-

28975-80-6
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Yield:-

Reaction Conditions:

with water;acetic acid in methanol at 37; pH=7.4;Kinetics;

Steps:

1

The rates of release of NE-2,4-dinitrophenyl-L-lysine from these compounds were determined at pH 7.4 or pH 8.3, 37°C, by HPLC analysis. Kinetic analyses of the release reactions were performed by HPLC (C18; linear MeOH/water + 0.5% HOAc gradient) using a UV/vis monitor at 350 nm. The areas under the Lys(DNP) ("P") and starting material ("S") peaks were integrated to determine extent of reaction("R") as R = P/(S+P). Reaction rates were calculated from the slope the line obtained by linear regression analysis of a plot of ln(l-R) versus time. The t]/2 values of β-eliminative cleavage of DNP-Lys carbamates at pH 7.4 and/or 8.3 are shown in Table 2.

References:

WO2011/140392,2011,A1 Location in patent:Page/Page column 31-32