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[4-(2,4-dihydro-1H-3,1-benzoxazin-2-yl)phenyl]-dimethyl-amine

Compound with spectra: 2 NMR, and 2 MS (GC)

[4-(2,4-dihydro-1H-3,1-benzoxazin-2-yl)phenyl]-dimethyl-amine
SpectraBase Compound ID 8GM2JPfXrKh
InChI InChI=1S/C16H18N2O/c1-18(2)14-9-7-12(8-10-14)16-17-15-6-4-3-5-13(15)11-19-16/h3-10,16-17H,11H2,1-2H3
InChIKey CXHDDLKBGZZMPQ-UHFFFAOYSA-N
Mol Weight 254.33 g/mol
Molecular Formula C16H18N2O
Exact Mass 254.141913 g/mol

View Spectrum of [4-(2,4-dihydro-1H-3,1-benzoxazin-2-yl)phenyl]-dimethyl-amine

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum G1-0-0-0

View Spectrum of [4-(2,4-dihydro-1H-3,1-benzoxazin-2-yl)phenyl]-dimethyl-amine

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum O-26-442-2

View Spectrum of [4-(2,4-dihydro-1H-3,1-benzoxazin-2-yl)phenyl]-dimethyl-amine

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3;0.2M

View Spectrum of [4-(2,4-dihydro-1H-3,1-benzoxazin-2-yl)phenyl]-dimethyl-amine

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6;0.2M
  • (4H)3,1-Benzoxazine, 2-[4-(dimethylamino)phenyl]-1,2-dihydro-
2-(4-methoxyphenyl)-2,4-dihydro-1H-3,1-benzoxazine
4-(2,4-dihydro-1H-3,1-benzoxazin-2-yl)benzonitrile
MRNACCOMMUJMCY-BVGQSLNGSA-N
2-[p-(dimethylamino)phenyl]benzothiazoline
N,N-dimethyl-4-((2R,4aS,8aR)-octahydro-1H-benzo[d][1,3]oxazin-2-yl)aniline
N,N-dimethyl-4-((2S,4aS,8aS)-octahydro-1H-benzo[d][1,3]oxazin-2-yl)aniline
2-(4-Methoxy-phenyl)-1,2,3,4-tetrahydro-quinoline
1,4-Dihydro-2H-(3,1)-benzoxazin-2-spiro[1'-cyclohexane]
1,4-Dihydro-2H-(3,1)-benzoxazin-2-spiro[1'-cyclopentane]
N,N-dimethyl-4-((2R,4aR,8aS)-octahydro-2H-benzo[e][1,3]oxazin-2-yl)aniline
Title Journal or Book Year
Substituent Influences on the Stability of the Ring and Chain Tautomers in 1,3-O,N-Heterocyclic Systems:  Characterization by 13C NMR Chemical Shifts, PM3 Charge Densities, and Isodesmic Reactions The Journal of Organic Chemistry 2001
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