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N-Phenyl-9-azabicyclo[3.3.1]nonane-9-carboxamide

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

N-Phenyl-9-azabicyclo[3.3.1]nonane-9-carboxamide
SpectraBase Compound ID IiVsVGU6L1z
InChI InChI=1S/C15H20N2O/c18-15(16-12-6-2-1-3-7-12)17-13-8-4-9-14(17)11-5-10-13/h1-3,6-7,13-14H,4-5,8-11H2,(H,16,18)/t13-,14+
InChIKey DFUXJBPLSFQVBU-OKILXGFUSA-N
Mol Weight 244.34 g/mol
Molecular Formula C15H20N2O
Exact Mass 244.157563 g/mol

View Spectrum of N-Phenyl-9-azabicyclo[3.3.1]nonane-9-carboxamide

MS (GC) Spectrum
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Source of Spectrum J-58-7088-7

View Spectrum of N-Phenyl-9-azabicyclo[3.3.1]nonane-9-carboxamide

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Thiourea, N,N-dicyclohexyl-N'-phenyl-
2-methyl-1-piperidinecarboxanilide
1-cyclohexyl-3-(p-methoxyphenyl)-1-methylurea
1-Cyclohexyl-5-methyl-2-imidazolidinone
N-METHOXYCARBONYL-9-AZABICYCLO-[3.3.1]-AND-[4.2.1]-NONANE;(RATIO=1:1)
4'-chloro-3-methyl-1-piperidinecarboxanilide
1-(1-ethynylcyclohexyl)-3-phenylurea
1,1-diisopropyl-3-(m-methoxyphenyl)urea
3(2H)-Indolizinone, hexahydro-5-propyl-, cis-
(5R,8aR)-5-propyl-2,5,6,7,8,8a-hexahydro-1H-indolizin-3-one
Title Journal or Book Year
Transannular reactions of cycloalkenes, cycloalkadienes, and cycloalkatrienes. 17. N-Heterocyclization in electrophilic haloamidation reactions of 1,5-cyclooctadiene. Synthesis and rearrangements of the granatanine and homonortropane skeletons The Journal of Organic Chemistry 1993
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