-
2-iodo-4-phenylphenol Molecule
InChIKey RXRDOSHIMLSXKG-UHFFFAOYSA-N Molecular Formula C12H9IO
Related Dataset(s)
-
2-methoxy-4-prop-2-enylphenol Molecule
InChIKey RRAFCDWBNXTKKO-UHFFFAOYSA-N Molecular Formula C10H12O2
Related Dataset(s)
- EUGENOL.c13
- Eugenol 400 MHz CDCl3 NMR data.1d
- EUGENOL; EI-B; MS
- Eugenol 400 MHz CDCl3 NMR data.cosy
- Eugenol 400 MHz CDCl3 NMR data[Eugenol_8070ug200uL_CDCl3_qHNMR_400MHz_Jeol.jdf]
- Eugenol 400 MHz CDCl3 NMR data[Eugenol_8070ug200uL_CDCl3_COSY_400MHz_Jeol.jdf]
- EUGENOL.hsqc
- EUGENOL.noesy
- Eugenol 400 MHz CDCl3 NMR data.
- EUGENOL.hmbc
- Classics_Eugenol.jres
- Classics_Eugenol[8]
- EUGENOL; EI-B; MS
- Classics_Eugenol[5]
- Eugenol 400 MHz CDCl3 NMR data[Eugenol_8070ug200uL_CDCl3_13CNMR_400MHz_Jeol.jdf]
- Eugenol; LC-ESI-QTOF; MS2; [M+H]+; CE: 20eV
- Classics_Eugenol[1]
- EUGENOL; EI-B; MS
- 2-METHOXY-4-(2-PROPENYL)PHENOL; EI-B; MS
- Classics_Eugenol[4]
- EUGENOL.cosy
- EUGENOL; EI-B; MS
- Eugenol; LC-ESI-QTOF; MS2; [M+H]+; CE: 50eV
- Eugenol 400 MHz CDCl3 NMR data.hmbc
- Eugenol 400 MHz CDCl3 NMR data[Eugenol_8070ug200uL_CDCl3_HSQC_400MHz_Jeol.jdf]
- EUGENOL.proton
- Eugenol; LC-ESI-QTOF; MS2; [M+H]+; CE: 10eV
- Eugenol 400 MHz CDCl3 NMR data.2d
- Eugenol; LC-ESI-QTOF; MS2; [M+H]+; CE: 30eV
- Eugenol 400 MHz CDCl3 NMR data.hsqc
- Eugenol; LC-ESI-QTOF; MS2; [M+H]+; CE: 40eV
- Classics_Eugenol[3]
- Classics_Eugenol[6]
- EUGENOL; EI-B; MS
- Classics_Eugenol[2]
-
2-methyl-2,3-dihydropyran-6-one Molecule
InChIKey DYNKRGCMLGUEMN-UHFFFAOYSA-N Molecular Formula C6H8O2
Related Dataset(s)
-
2-methyl-5-propan-2-ylcyclohexa-2,5-diene-1,4-dione Molecule
InChIKey KEQHJBNSCLWCAE-UHFFFAOYSA-N Molecular Formula C10H12O2
Related Dataset(s)
-
2-methyl-6-methylideneocta-2,7-dien-4-ol Molecule
InChIKey NHMKYUHMPXBMFI-UHFFFAOYSA-N Molecular Formula C10H16O
Related Dataset(s)
- 14434-41-4[dept135.dx]
- 14434-41-4[13c.fid.dx]
- 14434-41-4[1h.dx]
- 2-METHYL-6-METHYLENE-2,7-OCTADIEN-4-OL; EI-B; MS
- 14434-41-4[hmbc.ser.dx]
- 14434-41-4[hmbc.dx]
- 14434-41-4[13c.dx]
- 14434-41-4[hmqc.dx]
- 14434-41-4[1h.fid.dx]
- 14434-41-4[dept135.fid.dx]
- 14434-41-4[hmqc.ser.dx]
- 14434-41-4[cosy.ser.dx]
- 14434-41-4[cosy.dx]
-
21-hydroxy-16,17-dimethoxy-6-prop-1-en-2-yl-2,7,20-trioxapentacyclo[11.8.0.03... Molecule
InChIKey OFLJOIFZMITSOL-UHFFFAOYSA-N Molecular Formula C23H22O7
Related Dataset(s)
- YAC_3M (Compound 15) 6-Hydroxyrotenone[16]
- YAC_3M (Compound 15) 6-Hydroxyrotenone[11]
- YAC_3M (Compound 15) 6-Hydroxyrotenone[17]
- YAC_3M (Compound 15) 6-Hydroxyrotenone[14]
- YAC_3M (Compound 15) 6-Hydroxyrotenone[15]
- YAC_3M (Compound 15) 6-Hydroxyrotenone[13]
- YAC_3M (Compound 15) 6-Hydroxyrotenone[12]
- YAC_3M (Compound 15) 6-Hydroxyrotenone[99999]
-
3,4,5-trihydroxybenzoic acid Molecule
InChIKey LNTHITQWFMADLM-UHFFFAOYSA-N Molecular Formula C7H6O5
Related Dataset(s)
- Gallic acid; LC-ESI-QTOF; MS2
- Gallic acid; LC-ESI-QQ; MS2; CE:20 V; [M-H]-
- Gallic acid; LC-ESI-QTOF; MS2
- Gallic acid annotated NMR 400 MHz DMSOd6 data[13C.jdx]
- Gallic acid; LC-ESI-QTOF; MS2
- Gallic acid; LC-ESI-QTOF; MS2
- Gallic acid annotated NMR 400 MHz DMSOd6 data[HMBC.jdx]
- Gallic acid annotated NMR 400 MHz DMSOd6 data[HSQC.jdx]
- Gallic acid; LC-ESI-QQ; MS2; CE:50 V; [M-H]-
- Gallic acid; LC-ESI-QQ; MS2; CE:40 V; [M-H]-
- Gallic acid annotated NMR 400 MHz DMSOd6 data[13C.jdf]
- Gallic acid; LC-ESI-QTOF; MS2
- Gallic acid; LC-ESI-QTOF; MS2
- Gallic acid; LC-ESI-QTOF; MS2
- Gallic acid; GC-EI-TOF; MS; n TMS; RT:749.744 sec
- Gallic acid; LC-ESI-QTOF; MS2
- Gallic acid annotated NMR 400 MHz DMSOd6 data[1H.jdf]
- Gallic acid annotated NMR 400 MHz DMSOd6 data[COSY.jdx]
- Gallic acid annotated NMR 400 MHz DMSOd6 data[COSY.jdf]
- Gallic acid; LC-ESI-QTOF; MS2
- Gallic acid; LC-ESI-QTOF; MS2
- Gallic acid; LC-ESI-QTOF; MS2
- Gallic acid; LC-ESI-QTOF; MS2
- Gallic acid annotated NMR 400 MHz DMSOd6 data[HSQC.jdf]
- Gallic acid; LC-ESI-QTOF; MS2
- 3,4,5-TRIHYDROXYBENZOIC ACID; EI-B; MS
- Gallic acid; LC-ESI-QTOF; MS2
- Gallic acid; LC-ESI-QQ; MS2
- Gallic acid; LC-ESI-QTOF; MS2
- Gallic acid; LC-ESI-QTOF; MS2
- Gallic acid; LC-ESI-QTOF; MS2
- Gallic acid; LC-ESI-QQ; MS2; CE:30 V; [M-H]-
- Gallic acid; LC-ESI-QTOF; MS2
- Gallic acid; LC-ESI-QTOF; MS2
- Gallic acid; LC-ESI-QTOF; MS2
- Gallic acid; LC-ESI-QTOF; MS2
- Gallic acid; LC-ESI-QTOF; MS2
- Gallic acid; LC-ESI-QQ; MS2; CE:10 V; [M-H]-
- Gallic acid annotated NMR 400 MHz DMSOd6 data[HMBC.jdf]
- Gallic acid; LC-ESI-QTOF; MS2
- Gallic acid annotated NMR 400 MHz DMSOd6 data[1H.jdx]
- Gallic acid; LC-ESI-QTOF; MS2
- Gallic acid; LC-ESI-QTOF; MS2
-
3,5,6,8-tetrahydroxy-1-methyl-9,10-dioxo-7-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy... Molecule
InChIKey DGQLVPJVXFOQEV-JNVSTXMASA-N Molecular Formula C22H20O13
Related Dataset(s)
- Carminic acid; LC-ESI-QFT; MS2; CE: 45; R=17500; [M-H]-
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- NMR_Bruker-FID[5]
- electrospray ionisation tandem mass spectrometry (ESI-MS2)
- ultraviolet-visible spectrophotometry (UV-VIS)
- Carminic acid; LC-ESI-QFT; MS2; CE: 15; R=17500; [M-H]-
- Carminic acid; LC-ESI-QFT; MS2; CE: 60; R=17500; [M-H]-
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- circular dichroism spectroscopy (CD spectrometry)
- NMR_Bruker-FID[2]
- Carminic acid; LC-ESI-QFT; MS2; CE: 75; R=17500; [M-H]-
- ultraviolet-visible spectrophotometry (UV-VIS)
- ultraviolet-visible spectrophotometry (UV-VIS)
- NMR_Bruker-FID[3]
- NMR_Bruker-FID[4]
- Carminic acid; LC-ESI-QFT; MS2; CE: 30; R=17500; [M-H]-
- 1H--1H nuclear Overhauser enhancement spectroscopy (1H-1H NOESY)
- NMR_Bruker-FID[6]
- 1H--1H correlation spectroscopy (1H-1H COSY)
- Carminic acid; LC-ESI-QFT; MS2; CE: 90; R=17500; [M-H]-
- NMR_Bruker-FID[1]
- 1H--13C heteronuclear multiple bond coherence (13C-1H HMBC)
- 1H--13C heteronuclear single quantum coherence (1H-13C HSQC)
-
3,5,7-trihydroxy-2-(4-hydroxyphenyl)chromen-4-one Molecule
InChIKey IYRMWMYZSQPJKC-UHFFFAOYSA-N Molecular Formula C15H10O6
Related Dataset(s)
- Kaempferol; LC-ESI-QQ; MS2
- Kaempferol; LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
- Kaempferol; LC-ESI-QTOF; MS2
- Kaempferol; LC-ESI-QQ; MS2; CE:35 eV; [M+H]+
- Kaempferol; LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
- Kaempferol; LC-ESI-QTOF; MS2; CE:15 eV; [M+H]+
- Kaempferol; LC-ESI-QTOF; MS2; CE:30 eV; [M-H]-
- Kaempferol; LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
- Kaempferol; LC-ESI-QTOF; MS2
- Kaempferol; LC-ESI-QTOF; MS2; CE: 10; R=; [M+H]+
- Kaempferol; LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
- kaempferol; LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
- Kaempferol; LC-ESI-QQ; MS2; CE:40 eV; [M-H]-
- Kaempferol; LC-ESI-QTOF; MS2; CE 10 ev; [M-H]-
- Kaempferol annotated NMR 400 MHz DMSOd6 data[1H.jdx]
- Kaempferol; LC-ESI-QTOF; MS2
- Kaempferol; LC-ESI-QTOF; MS2; CE:40 eV; [M+H]+
- Kaempferol; LC-ESI-QTOF; MS2; CE:Ramp 5-60 eV; [M+H]+
- Kaempferol; LC-ESI-QFT; MS2; CE: 30; R=17500; [M-H]-
- Kaempferol; LC-ESI-ITTOF; MS; [M-H]-
- Kaempferol; LC-ESI-ITFT; MS2; CE: 65%; R=15000; [M+H]+
- Kaempferol; LC-ESI-ITFT; MS2; CE: 95%; R=15000; [M+H]+
- Kaempferol annotated NMR 400 MHz DMSOd6 data[13C.jdx]
- Kaempferol; LC-ESI-ITFT; MS2; CE 45 eV; [M+H]+
- Kaempferol; LC-ESI-QTOF; MS2; CE:30 eV; [M+H]+
- Kaempferol; LC-ESI-QTOF; MS2
- Kaempferol; LC-ESI-QFT; MS2; CE: 90; R=17500; [M-H]-
- Kaempferol; LC-ESI-QTOF; MS2
- Kaempferol; LC-ESI-ITFT; MS2; CE: 25%; R=15000; [M+H]+
- Kaempferol; LC-ESI-QQ; MS2; CE:35 eV; [M-H]-
- 4',5,7-TRIHYDROXYFLAVONOL; EI-B; MS
- Kaempferol; LC-ESI-QTOF; MS2; CE:55 eV; [M+H]+
- Kaempferol; LC-ESI-ITFT; MS2; CE: 105%; R=15000; [M+H]+
- Kaempferol; LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
- Kaempferol; LC-ESI-ITFT; MS2; CE 55 eV; [M+H]+
- Kaempferol annotated NMR 400 MHz DMSOd6 data[COSY.jdf]
- Kaempferol; LC-ESI-QTOF; MS2; CE:30 eV; [M+H]+
- Kaempferol; LC-ESI-QTOF; MS2
- Kaempferol; LC-ESI-QTOF; MS2
- Kaempferol; LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
- Kaempferol annotated NMR 400 MHz DMSOd6 data[HSQC.jdx]
- Kaempferol; LC-ESI-QTOF; MS
- Kaempferol; LC-ESI-QTOF; MS2; CE:Ramp 5-60 eV; [M-H]-
- Kaempferol; LC-ESI-QTOF; MS2
- Kaempferol; LC-ESI-QTOF; MS2
- Kaempferol; LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
- Keampferol; ESI-TOF; MS2; CE:15 eV; [M+H]+
- Kaempferol; LC-ESI-QTOF; MS2
- Indigo yellow, Popuinetin, 3,5,7-trihydroxy-2-(4-hydroxyphenyl)chromen-4-one, 4H-1-Benzopyran-4-one, 5,7,4'-Trihydroxyflavonol, Trifolitin, pelargidenolon, Kaem, Kampherol, 3,5,7-trihydroxy-2-(4-hydroxyphenyl)-5,7,4'-Trihydroxyflavonol, nimbecetin, Kaempferol, rhamnolutein, Robigenin, Rhamnolutin, 3,4',5,7-tetrahydroxyflavone, Populnetin, Kempferol, Swartziol; LC-ESI-QTOF; MS2
- Kaempferol; LC-ESI-QTOF; MS2; CE:15 eV; [M+H]+
- Kaempferol; LC-ESI-QTOF; MS2; CE:50 eV; [M-H]-
- Indigo yellow, Popuinetin, 4H-1-Benzopyran-4-one, 5,7,4'-Trihydroxyflavonol, Trifolitin, pelargidenolon, Kaem, Kampherol, 3,5,7-trihydroxy-2-(4-hydroxyphenyl)-5,7,4'-Trihydroxyflavonol, nimbecetin, Kaempferol, rhamnolutein, Robigenin, Rhamnolutin, 3,4',5,7-tetrahydroxyflavone, Populnetin, Kempferol, Swartziol; LC-ESI-QQ; MS2
- Kaempferol; LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
- Kaempferol; LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
- Kaempferol; LC-ESI-QTOF; MS2; CE 20 ev; [M-H]-
- Kaempferol; LC-ESI-QTOF; MS2
- Kaempferol; LC-ESI-QTOF; MS2; CE:25 eV; [M+H]+
- Kaempferol annotated NMR 400 MHz DMSOd6 data[1H.jdf]
- Kaempferol annotated NMR 400 MHz DMSOd6 data[13C.jdf]
- Kaempferol; LC-ESI-QFT; MS2; CE: 75; R=17500; [M-H]-
- Kaempferol; LC-ESI-QTOF; MS; POSITIVE
- Kaempferol; LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
- Kaempferol; LC-ESI-QTOF; MS2
- Kaempferol; LC-ESI-QTOF; MS2; CE: 40; R=; [M+H]+
- Kaempferol; LC-ESI-QQ; MS2
- Indigo yellow, Popuinetin, 4H-1-Benzopyran-4-one, 5,7,4'-Trihydroxyflavonol, Trifolitin, pelargidenolon, Kaem, Kampherol, 3,5,7-trihydroxy-2-(4-hydroxyphenyl)-5,7,4'-Trihydroxyflavonol, nimbecetin, Kaempferol, rhamnolutein, Robigenin, Rhamnolutin, 3,4',5,7-tetrahydroxyflavone, Populnetin, Kempferol, Swartziol; LC-ESI-QQ; MS2
- Kaempferol; LC-ESI-QFT; MS2; CE: 15; R=17500; [M-H]-
- Kaempferol annotated NMR 400 MHz DMSOd6 data[HMBC.jdf]
- Kaempferol; LC-ESI-QQ; MS2; CE:30 eV; [M-H]-
- Kaempferol; LC-ESI-QTOF; MS2
- Kaempferol annotated NMR 400 MHz DMSOd6 data[HMBC.jdx]
- Kaempferol; LC-ESI-QTOF; MS2
- Kaempferol annotated NMR 400 MHz DMSOd6 data[HSQC.jdf]
- Kaempferol; LC-ESI-QFT; MS2; CE: 45; R=17500; [M-H]-
- Kaempferol; LC-ESI-QTOF; MS2
- Kaempferol; LC-ESI-ITFT; MS2; CE: 100%; R=15000; [M+H]+
- Kaempferol; LC-ESI-QTOF; MS2
- Kaempferol; LC-ESI-QTOF; MS2; CE:10 eV; [M+H]+
- Kaempferol; LC-ESI-QTOF; MS2
- Kaempferol annotated NMR 400 MHz DMSOd6 data[COSY.jdx]
- Kaempferol; LC-ESI-ITFT; MS2; CE: 85%; R=15000; [M+H]+
- Kaempferol; LC-ESI-QTOF; MS2; CE: 20; R=; [M+H]+
- Kaempferol; LC-ESI-QTOF; MS2; CE:20 eV; [M-H]-
- Kaempferol; LC-ESI-ITFT; MS2; CE: 10%; R=15000; [M+H]+
- Kaempferol; LC-ESI-QTOF; MS2; CE:Ramp 5-60 V; [M-H]-
- Kaempferol; LC-ESI-QTOF; MS2; CE:25 eV; [M+H]+
- Kaempferol; LC-ESI-QTOF; MS2
- Kaempferol; LC-ESI-ITFT; MS2; CE: 55%; R=15000; [M+H]+
- Indigo yellow, Popuinetin, 4H-1-Benzopyran-4-one, 5,7,4'-Trihydroxyflavonol, Trifolitin, pelargidenolon, Kaem, Kampherol, 3,5,7-trihydroxy-2-(4-hydroxyphenyl)-5,7,4'-Trihydroxyflavonol, nimbecetin, Kaempferol, rhamnolutein, Robigenin, Rhamnolutin, 3,4',5,7-tetrahydroxyflavone, Populnetin, Kempferol, Swartziol; LC-ESI-QQ; MS2
- Kaempferol; LC-ESI-QTOF; MS2; CE:20 eV; [M+H]+
- Kaempferol; LC-ESI-QQ; MS2; CE:30 eV; [M+H]+
- Kaempferol; LC-ESI-QTOF; MS2; CE:Ramp 5-60 V; [M+H]+
- Kaempferol; LC-ESI-ITFT; MS2; CE 35 eV; [M+H]+
- Kaempferol; LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
- Kaempferol; LC-ESI-QTOF; MS2
- Kaempferol; LC-APCI-QTOF; MS; NEGATIVE
- Keampferol; ESI-TOF; MS2; CE:15 eV; [M+H]+
- Kaempferol; LC-ESI-QQ; MS2; CE:25 eV; [M+H]+
- Kaempferol; LC-ESI-QTOF; MS; NEGATIVE
- Kaempferol; LC-ESI-QTOF; MS2
- Kaempferol; LC-ESI-QTOF; MS2
- Kaempferol; LC-ESI-QTOF; MS2
- Kaempferol; LC-ESI-ITFT; MS; [M+H]+; isotope pattern
- Kaempferol; LC-ESI-QTOF; MS
- Kaempferol; LC-ESI-QTOF; MS2
- Flavonol base + 3O; LC-ESI-QTOF; MS2
- Kaempferol; LC-ESI-QFT; MS2; CE: 60; R=17500; [M-H]-
- Kaempferol; GC-EI-TOF; MS; n TMS; RT:1106.633 sec
- Kaempferol; LC-ESI-QTOF; MS2; CE 40 ev; [M-H]-
- Kaempferol; LC-ESI-QTOF; MS2
- Indigo yellow, Popuinetin, 3,5,7-trihydroxy-2-(4-hydroxyphenyl)chromen-4-one, 4H-1-Benzopyran-4-one, 5,7,4'-Trihydroxyflavonol, Trifolitin, pelargidenolon, Kaem, Kampherol, 3,5,7-trihydroxy-2-(4-hydroxyphenyl)-5,7,4'-Trihydroxyflavonol, nimbecetin, Kaempferol, rhamnolutein, Robigenin, Rhamnolutin, 3,4',5,7-tetrahydroxyflavone, Populnetin, Kempferol, Swartziol; LC-ESI-QTOF; MS2
- Indigo yellow, Popuinetin, 4H-1-Benzopyran-4-one, 5,7,4'-Trihydroxyflavonol, Trifolitin, pelargidenolon, Kaem, Kampherol, 3,5,7-trihydroxy-2-(4-hydroxyphenyl)-5,7,4'-Trihydroxyflavonol, nimbecetin, Kaempferol, rhamnolutein, Robigenin, Rhamnolutin, 3,4',5,7-tetrahydroxyflavone, Populnetin, Kempferol, Swartziol; LC-ESI-QQ; MS2
- Kaempferol; LC-APCI-QTOF; MS; POSITIVE
- Kaempferol; LC-ESI-QTOF; MS2
- Kaempferol; LC-ESI-QTOF; MS2; CE:40 eV; [M-H]-
- Kaempferol; LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
- Kaempferol; LC-ESI-QTOF; MS2
-
3,7-dimethylocta-1,6-dien-3-ol Molecule
InChIKey CDOSHBSSFJOMGT-UHFFFAOYSA-N Molecular Formula C10H18O
Related Dataset(s)
- Rutin 400 MHz in DMSOd6 NMR data[Rutin_3080ug200uL_DMSOd6_HSQC_400MHz_JDX.jdx]
- Linalool 60/400/900 MHz in CDCl3 NMR data.
- Linalool 60/400/900 MHz in CDCl3 NMR data.1d
- Rutin 400 MHz in DMSOd6 NMR data[Rutin_3080ug200uL_DMSOd6_COSY_400MHz_Jeol.jdf]
- Rutin 400 MHz in DMSOd6 NMR data[Rutin_3080ug200uL_DMSOd6_13CNMR_400MHz_Jeol.jdf]
- LINALOOL; EI-B; MS
- Linalool 60/400/900 MHz in CDCl3 NMR data.2d
- Linalool 60/400/900 MHz in CDCl3 NMR data[Linalool_100000ug200uL_CDCl3_1HNMR_900MHz_JDX.jdx]
- Linalool 60/400/900 MHz in CDCl3 NMR data[Linalool_3289ug200uL_CDCl3_13C_400MHz_Jeol.jdf]
- Rutin 400 MHz in DMSOd6 NMR data[Rutin_3080ug200uL_DMSOd6_qHNMR_400MHz_JDX.jdx]
- Linalool 60/400/900 MHz in CDCl3 NMR data.hsqc
- Linalool 60/400/900 MHz in CDCl3 NMR data.hmbc
- Linalool 60/400/900 MHz in CDCl3 NMR data.2d
- Rutin 400 MHz in DMSOd6 NMR data[Rutin_3080ug200uL_DMSOd6_HMBC_400MHz_Jeol.jdf]
- Linalool 60/400/900 MHz in CDCl3 NMR data.cosy
- Rutin 400 MHz in DMSOd6 NMR data[Rutin_3080ug200uL_DMSOd6_HMBC_400MHz_JDX.jdx]
- Linalool 60/400/900 MHz in CDCl3 NMR data.
- Linalool 60/400/900 MHz in CDCl3 NMR data.2d
- Rutin 400 MHz in DMSOd6 NMR data[Rutin_3080ug200uL_DMSOd6_HSQC_400MHz_Jeol.jdf]
- Linalool 60/400/900 MHz in CDCl3 NMR data.1d
- LINALOOL; EI-B; MS
- Rutin 400 MHz in DMSOd6 NMR data[Rutin_3080ug200uL_DMSOd6_qHNMR_400MHz_Jeol.jdf]
- Linalool 60/400/900 MHz in CDCl3 NMR data.cosy
- Rutin 400 MHz in DMSOd6 NMR data[Rutin_3080ug200uL_DMSOd6_13CNMR_400MHz_JDX.jdx]
- Rutin 400 MHz in DMSOd6 NMR data[Rutin_3080ug200uL_DMSOd6_COSY_400MHz_JDX.jdx]
-
3,9-bis[(4-buta-2,3-dienoxyphenyl)methyl]-1,7-dimethyl-6,12-bis(2-methylpropy... Molecule
InChIKey QWMKZQLCKVCIIN-UHFFFAOYSA-N Molecular Formula C40H52N4O6
Related Dataset(s)
-
3-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-(3-hydroxy-3-methylbutyl)chromen-4-one Molecule
InChIKey QATXOFGLOAQGRT-UHFFFAOYSA-N Molecular Formula C20H20O7
Related Dataset(s)
-
3-hydroxy-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthre... Molecule
InChIKey MGSYUDDLXLZUOM-UHFFFAOYSA-N Molecular Formula C20H30O3
Related Dataset(s)
-
3-hydroxy-5-methoxy-5-phenacyl-4-phenylfuran-2-one Molecule
InChIKey ZSQDINYGPVLTCM-UHFFFAOYSA-N Molecular Formula C19H16O5
Related Dataset(s)
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- double-quantum-filtered correlation spectroscopy (DQF-COSY)
- two-dimensional nuclear Overhauser enhancement spectroscopy (2D NOESY)
- Allantofuranone (1155308-25-0)[13c.dx]
- high-resolution electrospray ionisation time-of-flight mass spectrometry (HR-ESI-TOF-MS)
- 1H--13C heteronuclear single quantum coherence (1H-13C HSQC)
- nuclear magnetic resonance spectroscopy (NMR)
- Allantofuranone (1155308-25-0)[cosy.dx]
- 1H--13C heteronuclear multiple bond coherence (13C-1H HMBC)
- Allantofuranone (1155308-25-0)[hsqc.dx]
- attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR)
- Allantofuranone (1155308-25-0)[1h.dx]
- Allantofuranone (1155308-25-0)[hmbc.dx]
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
-
4,5,7-trimethoxy-8-(3-methylbut-2-enyl)-2-phenyl-3,4-dihydro-2H-chromene Molecule
InChIKey QYAYIWOQUZDATC-UHFFFAOYSA-N Molecular Formula C23H28O4
Related Dataset(s)
-
4-(2,2,2-trifluoroethoxy)aniline Molecule
InChIKey OXFDNUZWKFKMSB-UHFFFAOYSA-N Molecular Formula C8H8F3NO
Related Dataset(s)
- 57946-61-9[19f1hdec.fid.dx]
- 57946-61-9[fh-cosy.ser.dx]
- 57946-61-9[hmqc.ser.dx]
- 57946-61-9[cosy.ser.dx]
- 57946-61-9[hmbc.ser.dx]
- 57946-61-9[hf-hoesy.ser.dx]
- 57946-61-9[1h.fid.dx]
- 57946-61-9[noesy.ser.dx]
- 57946-61-9[hf-hoesy.dx]
- 57946-61-9[19f1h-dec.dx]
- 4-2-2-2-trifluoroethoxy-benzenamine.hmqc
- 57946-61-9[noesy.dx]
- 57946-61-9[cosy.dx]
- 57946-61-9[hmbc.dx]
- 57946-61-9[deptq.fid.dx]
- 57946-61-9[deptq.dx]
- 57946-61-9[hmqc.dx]
- 57946-61-9[fh-cosy.dx]
- 57946-61-9[1h.dx]
-
4-[(2E)-3,7-dimethylocta-2,6-dienoxy]furo[3,2-g]chromen-7-one Molecule
InChIKey DBMJZOMNXBSRED-OQLLNIDSSA-N
Related Dataset(s)
- SI_Outreach_4_2D_1st_column_lime_extract_06012024_FULL[4]
- BERGAMOTTIN_FULL_NMR_THIX-029C2_2nd_col_4_1_Hex_EA_lime_peels_extract_06082024[5]
- SI_Outreach_4_2D_1st_column_lime_extract_06012024_FULL[6]
- SI_Outreach_4_2D_column_lime_05302024[2]
- SI_Outreach_4_2F_B_2nd_column_lime_05312024_FULL[2]
- SI_Outreach_4_2D_1st_column_lime_extract_06012024_FULL[5]
- SI_Outreach_5_1A_grapefruit_meat_05_31_2024[1]
- SI_Outreach_4_2D_column_lime_05302024.cosy
- SI_Outreach_4_2F_B_2nd_column_lime_05312024_FULL[5]
- SI_Outreach_4_2D_column_lime_05302024[1]
- BERGAMOTTIN_FULL_NMR_THIX-029C2_2nd_col_4_1_Hex_EA_lime_peels_extract_06082024[3]
- BERGAMOTTIN_FULL_NMR_THIX-029C2_2nd_col_4_1_Hex_EA_lime_peels_extract_06082024[4]
- SI_Outreach_4_2D_1st_column_lime_extract_06012024_FULL[7]
- SI_Outreach_4_2F_B_2nd_column_lime_05312024_FULL[3]
- SI_Outreach_4_2F_column_lime_05302024[1]
- SI_Outreach_4_2D_1st_column_lime_extract_06012024_FULL[2]
- SI_Outreach_4_4A_graprefruit_peels_05312024[1]
- SI_Outreach_4_2F_B_2nd_column_lime_05312024_FULL[1]
- SI_Outreach_4_2D_1st_column_lime_extract_06012024_FULL[3]
- SI_Outreach_4_2D_column_lime_05302024[3]
- BERGAMOTTIN_FULL_NMR_THIX-029C2_2nd_col_4_1_Hex_EA_lime_peels_extract_06082024[6]
- SI_Outreach_4_2D_column_lime_05302024[6]
- BERGAMOTTIN_FULL_NMR_THIX-029C2_2nd_col_4_1_Hex_EA_lime_peels_extract_06082024[1]
- SI_Outreach_4_2F_B_2nd_column_lime_05312024_FULL[6]
- SI_Outreach_4_2F_B_2nd_column_lime_05312024_FULL[4]
- SI_Outreach_4_2F_B_2nd_column_lime_05312024[1]
- SI_Outreach_4_2D_column_lime_05302024[4]
