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ETHYL-1-THIOXO-1H-PYRIDO-[1,2-C]-PYRIMIDINE-3-CARBOXYLATE

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

ETHYL-1-THIOXO-1H-PYRIDO-[1,2-C]-PYRIMIDINE-3-CARBOXYLATE
SpectraBase Compound ID GzP8UOFluN5
InChI InChI=1S/C11H10N2O2S/c1-2-15-10(14)9-7-8-5-3-4-6-13(8)11(16)12-9/h3-7H,2H2,1H3
InChIKey JOXSUGMGIRLYAO-UHFFFAOYSA-N
Mol Weight 234.27 g/mol
Molecular Formula C11H10N2O2S
Exact Mass 234.046299 g/mol

View Spectrum of ETHYL-1-THIOXO-1H-PYRIDO-[1,2-C]-PYRIMIDINE-3-CARBOXYLATE

MS (GC) Spectrum
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Source of Spectrum F-48-4611-13

View Spectrum of ETHYL-1-THIOXO-1H-PYRIDO-[1,2-C]-PYRIMIDINE-3-CARBOXYLATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
  • 1-sulfanylidene-3-pyrido[1,2-c]pyrimidinecarboxylic acid ethyl ester
ETHYL-2,3-DIHYDRO-2-OXOINDOLIZIN-1-ACETATE
2(3H)-indolizinone, 1-phenyl-
benzoic acid, 4-[(Z)-[3-[2-[[3-(dimethylamino)propyl]amino]-2-oxoethyl]-4-oxo-2-thioxo-5-thiazolidinylidene]methyl]-, methyl ester
(2Z,5Z)-(5-Ethoxycarbonylmethylidene-4-oxothiazolidin-2-ylidene)-1-phenyl-2-bromoethanone
(2S)-2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]-4-[2-oxo-4-(phenylmethoxycarbonylamino)-1-pyrimidinyl]butanoic acid methyl ester
8-Methoxy-5,6-isoquinolinedione
6-Methyl-4-phenyl-1-(p-tolyl)-2[1H]pyrimidinethione
RXTOFNWCKMRXBO-FUTHCOOYSA-N
4H-Pyrimido[1,2-a]pyrimidine-2-carboxylic acid, 4-oxo-, methyl ester
3-Trifluoroacetyl-1-phenyl-6-phenylamino-1,4,5,6-tetrahydropyridine
Title Journal or Book Year
Solid-Phase Synthesis and Inhibitory Effects of Some Pyrido[1,2-c]pyrimidine Derivatives on Leukocyte Functions and Experimental Inflammation Journal of Medicinal Chemistry 2001
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