Microdetermination of Bioethanomethrin

1975 ◽  
Vol 58 (4) ◽  
pp. 781-784
Author(s):  
Donald A George ◽  
Leslie M Mcdonough
Keyword(s):  
Spectral Data ◽  
Electron Capture ◽  
Synthetic Pyrethroid ◽  
Pyrethroid Insecticide ◽  
Electron Capture Detector ◽  
Gas Chromatograph ◽  
Mass Spectral Data ◽  
Acid Moiety ◽  
Mass Spectral

Abstract A microanalytical method was developed for the determination of the experimental synthetic pyrethroid insecticide Bioethanomethrin ((5- benzyl-3-furyl) methyl trans-(+)-3-( cyclopentylidenemethyl)-2,2 -dimethylcyclopropanecarboxylate). After saponification, trichloroacetyl chloride is used to form an ester from the alcohol moiety, and trichloroethanol is used to form an ester from the acid moiety. Infrared and mass spectral data support the expected structures of the derivatives formed. Nanogram sensitivity is realized by utilizing a gas chromatograph with an electron capture detector.

Mass spectral data for gas chromatograph-mass spectral identification of some irregular monoterpenes

1976 ◽  
Vol 21 (4) ◽  
pp. 500-502 ◽  
Author(s):  
William W. Epstein ◽  
Lawrence R. McGee ◽  
C. Dale Poulter ◽  
Larry L. Marsh
Keyword(s):  
Spectral Data ◽  
Gas Chromatograph ◽  
Mass Spectral Data ◽  
Mass Spectral ◽  
Spectral Identification

Synthesis, spectral description, and lipophilicity parameters determination of phenylcarbamic acid derivatives with integrated N-phenylpiperazine moiety in the structure

2006 ◽  
Vol 60 (1) ◽  
Author(s):  
I. Malík ◽  
E. Sedlárová ◽  
J. Csöllei ◽  
F. Andriamainty ◽  
P. Kurfürst ◽  
...  
Keyword(s):  
Neural Network ◽  
Spectral Data ◽  
1H Nmr ◽  
Elemental Analysis ◽  
Computer Programs ◽  
Mass Spectral Data ◽  
Mass Spectral ◽  
The Neural Network ◽  
Lipophilicity Parameters

AbstractThe phenylcarbamic acid derivatives with N-phenylpiperazine moiety in the molecule have been prepared. The structure has been confirmed by elemental analysis, IR, 1H NMR, and mass spectral data. For the prepared set of the compounds the lipophilicity parameters have been determined. The experimentally obtained lipophilicity parameters have been correlated with theoretical entries obtained by different computer programs based on the neural network and fragmental methods.

Structure determination of two structural analogs, named 3-[1-(2-fluoro-4-biphenyl)ethyl]-6-(4-fluorophenyl)-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazole (C23H16F2N4S) and 3-[1-(2-fluoro-4-biphenyl)ethyl]-6-(4-chlorophenyl)-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazole (C23H16ClFN4S) by synchrotron X-ray powder diffraction

2017 ◽  
Vol 32 (4) ◽  
pp. 279-289 ◽  
Author(s):  
Gülsüm Gündoğdu ◽  
Sevim Peri Aytaç ◽  
Melanie Müller ◽  
Birsen Tozkoparan ◽  
Filiz Betül Kaynak
Keyword(s):  
Spectral Data ◽  
Powder Diffraction ◽  
Cytotoxic Agents ◽  
Proton Nuclear Magnetic Resonance ◽  
Mass Spectral Data ◽  
Unit Cell Parameters ◽  
X Ray ◽  
Mass Spectral ◽  
Cell Parameters

Two novel compounds, 3-[1-(2-fluoro-4-biphenyl)ethyl]-6-(4-fluorophenyl)-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazole (C23H16F2N4S) (1) and 3-[1-(2-fluoro-4-biphenyl)ethyl]-6-(4-chlorophenyl)-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazole (C23H16ClFN4S) (2), have been designed and synthesized as cytotoxic agents. The compounds were characterized by infrared, proton nuclear magnetic resonance, mass spectral data, elemental analysis and X-ray powder diffraction. The present study comprises spectral data and crystal structures of these novel compounds determined from synchrotron X-ray powder diffraction data. The structure solutions were obtained by simulated annealing. The final structures were achieved by Rietveld refinement using soft restraints for all bond lengths, bond angles, and planar groups. Both compounds crystallize in space group $P\bar 1$, Z = 2, with the unit-cell parameters a = 6.37433(9), b = 11.3641(2), c = 14.09115(19) Å, α = 80.1740(8)°, β = 85.1164(8)°, γ = 80.9831(10)°, V = 991.55(3) Å3 of compound (1) and a = 6.53736(6), b = 11.55725(15), c = 14.01373(13) Å, α = 80.3323(7)°, β = 84.8939(6)°, γ = 79.3954(8)°, V = 1024.08(2) Å3 of compound (2). Structural analyses reveal that the title compounds are isostructural.

scholarly journals Green Synthetic Protocol for (E)-1-Aryl-3-(2-morpholinoquinolin- 3-yl)prop-2-en-1-ones and Their Antimicrobial Activity

2019 ◽  
Vol 31 (9) ◽  
pp. 1895-1898
Author(s):  
Relangi Siva Subrahmanyam ◽  
Venkateswara Rao Anna
Keyword(s):  
Antimicrobial Activity ◽  
Spectral Data ◽  
1H Nmr ◽  
13C Nmr ◽  
Mass Spectral Data ◽  
In Vitro Antimicrobial Activity ◽  
Mass Spectral ◽  
Fungal Organisms

We report here an easy, efficient and green synthetic protocol for the (E)-1-aryl-3-(2-morpholinoquinolin-3-yl)prop-2-en-1-ones by the Claisen-Schmidt condensation of 2-morpholinoquinoline-3-carbaldehyde and different substituted acetophenones by using 1-butyl-3-methylimidazolium tetrafluoroborate (Bmim)BF4. The compounds were characterized by using 1H NMR, 13C NMR and mass spectral data and screened there in vitro antimicrobial activity against different bacterial and fungal organisms.

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