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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
1,1-dicyclohexyl-3-phenylurea
1-cyclohexyl-1-isopropyl-3-phenylurea
Thiourea, N,N-dicyclohexyl-N'-phenyl-
2-methyl-1-piperidinecarboxanilide
1-cyclohexyl-3-(p-methoxyphenyl)-1-methylurea
2-(Hydroxymethyl)-N-phenyl-1-pyrrolidinecarboxamide
1-cyclohexyl-1-methyl-3-(p-nitrophenyl)urea
3-benzyl-1,1-dicyclohexylurea
DWQRXDGVENLJFC-UHFFFAOYSA-N
N'-(4-chlorophenyl)-N-methyl-N-(1-methyl-4-piperidinyl)urea
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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