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3-(4-METHOXYPHENYL)-2-CYANO-4-(5-METHYL-3-PHENETHYLTHIAZOLIN-2-YLIDENE)-BUT-2-ENENITRILE

Compound with spectra: 1 NMR, and 1 MS (GC)

3-(4-METHOXYPHENYL)-2-CYANO-4-(5-METHYL-3-PHENETHYLTHIAZOLIN-2-YLIDENE)-BUT-2-ENENITRILE
SpectraBase Compound ID 87c6ZSk9UyP
InChI InChI=1S/C24H21N3OS/c1-18-17-27(13-12-19-6-4-3-5-7-19)24(29-18)14-23(21(15-25)16-26)20-8-10-22(28-2)11-9-20/h3-11,14,17H,12-13H2,1-2H3/b24-14-
InChIKey HSETYEOIKDLHIK-OYKKKHCWSA-N
Mol Weight 399.51 g/mol
Molecular Formula C24H21N3OS
Exact Mass 399.140533 g/mol

View Spectrum of 3-(4-METHOXYPHENYL)-2-CYANO-4-(5-METHYL-3-PHENETHYLTHIAZOLIN-2-YLIDENE)-BUT-2-ENENITRILE

MS (GC) Spectrum
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Source of Spectrum Y-35-53-6

View Spectrum of 3-(4-METHOXYPHENYL)-2-CYANO-4-(5-METHYL-3-PHENETHYLTHIAZOLIN-2-YLIDENE)-BUT-2-ENENITRILE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 2-[(2Z)-1-(4-methoxyphenyl)-2-(5-methyl-3-phenethyl-4-thiazolin-2-ylidene)ethylidene]malononitrile
3-(4-BROMOPHENYL)-2-CYANO-4-(5-METHYL-3-PHENETHYLTHIAZOLIN-2-YLIDENE)-BUT-2-ENENITRILE
3-(4-CHLOROPHENYL)-2-CYANO-4-(5-METHYL-3-PHENETHYLTHIAZOLIN-2-YLIDENE)-BUT-2-ENENITRILE
3-(4-METHOXYPHENYL)-2-CYANO-4-(5-METHYLENE-3-PHENETHYLTHIAZOLIDIN-2-YLIDENE)-BUT-2-ENENITRILE
t-Butyl 2-[3',3'-dicyano-2'-(4"-methoxyphenyl)allylidene]-thiazolidine-3-carboxylate
t-Butyl 2-(3',3'-dicyano-2'-(4"-methylphenyl)allylidene)-perhydro-1,3-thiazine-3-carboxylate
(2Z)-2-(3,3-dicyano-2-phenyl-prop-2-enylidene)-1,3-thiazinane-3-carboxylic acid tert-butyl ester
YXJAFOZTPWSEFN-VXPUYCOJSA-N
2-keto-6-(p-anisidino)-4-phenyl-1H-pyridine-3-carbonitrile
2H-Thiopyran-5-carbonitrile, 6-amino-2-[(4-methoxyphenyl)imino]-4-phenyl-
3-Pyridinecarbonitrile, 1,2-dihydro-6-[(4-nitrophenyl)amino]-2-oxo-4-phenyl-
Title Journal or Book Year
Iminium carbonic acid derivative salts.XII. electrophilic reactions of 2-methylthio-4,5-dihydrothiazolium iodides, 5-methyl-2-methylthiothiazolium iodides and 2-methylthio-5,6-dihydro-1,3-thiazinium iodides. partIII. With Vinylogous and Phenylogous Active Methylene Compounds Journal of Heterocyclic Chemistry 1998

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