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dimethyl (2R)-2-({(2E)-3-[3,4-bis(acetyloxy)phenyl]prop-2-enoyl}oxy)butanedioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1363494-53-4

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1363494-53-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1363494-53-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,3,4,9 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1363494-53:
(9*1)+(8*3)+(7*6)+(6*3)+(5*4)+(4*9)+(3*4)+(2*5)+(1*3)=174
174 % 10 = 4
So 1363494-53-4 is a valid CAS Registry Number.

1363494-53-4Downstream Products

1363494-53-4Relevant academic research and scientific papers

An approach to the chemotaxonomic differentiation of two European Dog's mercury species: Mercurialis annua L. and M. perennis L.

Lorenz, Peter,Duckstein, Sarina,Conrad, Juergen,Knoedler, Matthias,Meyer, Ulrich,Stintzing, Florian C.

experimental part, p. 282 - 297 (2012/05/04)

Mercurialis annua and M. perennis are medicinal plants used in complementary medicine. In the present work, analytical methods to allow a chemotaxonomic differentiation of M. annua and M. perennis by means of chemical marker compounds were established. In addition to previously published compounds, the exclusive presence of pyridine-3-carbonitrile and nicotinamide in CH2Cl2 extracts obtained from the herbal parts of M. annua was demonstrated by GC/MS. Notably, pyridine-3-carbonitrile was identified for the first time as a natural product. Further chromatographic separation of the CH2Cl2 extracts via polyamide yielded a MeOH fraction exhibiting a broad spectrum of side-chain saturated n-alkylresorcinols. While the n-alkylresorcinol pattern was similar for both plant species, some specific differences were observed for particular n-alkylresorcinol homologs. Finally, the investigation of H2O extracts by LC/MS/MS revealed the presence of depside constituents. Whereas, in M. perennis, a mixture of mercurialis acid (=(2R)-[(E)-caffeoyl]-2-oxoglutarate) and phaselic acid (=(E)-caffeoyl-2-malate) could be detected, in M. annua solely phaselic acid was found. By comparison with synthesized enantiomerically pure (2R)- and (2S)-phaselic acids, the configuration of the depside could be determined as (2S) in M. annua and as (2R) in M. perennis.

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