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Endo-methyl-1-methyl-5-oxo-7-oxabicyclo-[2.2.1]-heptane-2-carboxylate

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

Endo-methyl-1-methyl-5-oxo-7-oxabicyclo-[2.2.1]-heptane-2-carboxylate
SpectraBase Compound ID CW2K5huY23w
InChI InChI=1S/C9H12O4/c1-9-4-6(10)7(13-9)3-5(9)8(11)12-2/h5,7H,3-4H2,1-2H3/t5-,7+,9+/m0/s1
InChIKey OPNOMEUTIMYNNS-MTQIGAJGSA-N
Mol Weight 184.19 g/mol
Molecular Formula C9H12O4
Exact Mass 184.073559 g/mol
Enantiomer InChIKey OPNOMEUTIMYNNS-SHRPOTNHSA-N

View Spectrum of Endo-methyl-1-methyl-5-oxo-7-oxabicyclo-[2.2.1]-heptane-2-carboxylate

Vapor Phase IR Spectrum
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View Spectrum of Endo-methyl-1-methyl-5-oxo-7-oxabicyclo-[2.2.1]-heptane-2-carboxylate

MS (GC) Spectrum
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum Y-59-338-5

View Spectrum of Endo-methyl-1-methyl-5-oxo-7-oxabicyclo-[2.2.1]-heptane-2-carboxylate

13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (1R,2R,4R)-1-Methyl-5-oxo-7-oxa-bicyclo[2.2.1]heptane-2-carboxylic acid methyl ester
  • Methyl (1R,2R,4R)-1-methyl-5-oxo-7-oxabicyclo[2.2.1]heptane-2-carboxylate
  • Methyl (endo)-1-methyl-5-oxo-7-oxabicyclo[2.2.1]heptane-2-carboxylate
EXO-METHYL-1-METHYL-5-OXO-7-OXABICYCLO-[2.2.1]-HEPTANE-2-CARBOXYLATE
Dimethyl 4,4-ethylenedioxycyclopentane-1,3-dicarboxylate
cis-Cyclohexanespiro-4'-[3'-(methoxycarbonyl)-2'-methyl-4'-butanolide]
trans-3-(Ethoxycarbonyl)-2-methyl-4-butanolide-4-spirocyclopentane
exo-2,3-Epoxy-exo-6-methoxycarbonyl-7-oxa-tricyclo(2.2.1)heptane
(R1,R4,R5,R6)-t-Butyl 5,6-dihydroxy-7-oxabicyclo[2.2.1]heptan-2-carboxylate
(1R,2S)-exo-3,6-Epoxy-2-(2-isopropoxycarbonyl)cyclohexane-1-carboxylic acid
(2S*)-2-(1-Hydroxy-1-methyl-3-phenylpropyl)-5-o-benzoyl-3-deoxyerythro-.gama.-lactone
2-Hydroxyheptadecane-1,2,3-tricarboxylic acid trimethyl ester
4H-1,3-Benzodioxin-4-one, 2-(1,1-dimethylethyl)hexahydro-5-(2-propenyl)-, [2S-(2.alpha.,4a.alpha.,5.beta.,8a.beta.)]-
Title Journal or Book Year
Diels - Alder Reactions of 3-Furylamines in Organic and Aqueous Solvents Australian Journal of Chemistry 2006
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