A new α-Tetralone based chalcone compound, (2E)-2-(4-ethoxybenzylidene)-3,4-dihydro-2H-naphthalen-1-one () has been synthesized by Claisen-Schmidt condensation reaction of α-Tetralone () with 4-Ethoxybenzaldehyde () in basic medium. Then it was allowed to grow through slow evaporation solution growth technique. The molecular structure of grown has been systematically characterized by SCXRD, FT-IR, H NMR and C NMR spectroscopic studies.
View Article and Find Full Text PDFComput Math Methods Med
June 2022
According to the Tamil Nadu Energy Development Agency (TEDA) in the 2019-20 academic year, the wind power plant produces 23% of the biomass power supply in the Indian electrical commodities. To maintain the power withstanding capability needed for future electrical commodities, a yearly power shutdown program is implemented. An additional wind power plant unit will be erected and create more electricity, thereby balancing India's commercial electricity needs.
View Article and Find Full Text PDFThe research received a great deal of worldwide attention due to the nature of interpretation before the experimental process. Based on the systematic process the structure of thiazole -pyrazole compound 4-[{2-[3-(4-chlorophenyl)-5-(4-propan-2-yl) phenyl)-4, 5-dihydro- 1H- pyrazol-1-yl]-4-oxo-1, 3- thiazol-5(4H)-ylidene} methyl] benzonitrile [CPTBN] was investigated. In the first level, the spectral statistics on experimental FT-IR and FT- Raman was reported.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
April 2020
The title compound, CHClNO, contains a methyl-piperidine ring in the stable chair conformation. The mean plane of the twisted piperidine ring subtends a dihedral angle of 39.89 (7)° with that of the benzene ring.
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
February 2018
Experimental FT-IR and FT-Raman spectra of 2-methylphenylacetic acid (MPA) were recorded and theoretical values are also analyzed. The non-linear optical (NLO) properties were evaluated by determination of first (5.5053×10 e.
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