-
3-hydroxybenzoic acid Molecule
InChIKey IJFXRHURBJZNAO-UHFFFAOYSA-N Molecular Formula C7H6O3
Related Dataset(s)
- 1H--13C heteronuclear multiple bond coherence (13C-1H HMBC)
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- 3-hydroxybenzoic acid; LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
- m-Hydroxybenzoic acid; LC-ESI-QQ; MS2; CE:30 V; [M-H]-
- 1H--1H correlation spectroscopy (1H-1H COSY)
- META-HYDROXYBENZOIC ACID; EI-B; MS
- 1H--13C heteronuclear single quantum coherence (1H-13C HSQC)
- m-Hydroxybenzoic acid; LC-ESI-QQ; MS2; CE:50 V; [M-H]-
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- m-Hydroxybenzoic acid; LC-ESI-QQ; MS2; CE:40 V; [M-H]-
- 3-HydroxyBenzoic acid; EI-B; MS; 2 TMS; RT: 619.07 s
- m-Hydroxybenzoic acid; LC-ESI-QQ; MS2; CE:10 V; [M-H]-
- m-Hydroxybenzoic acid; LC-ESI-QQ; MS2; CE:20 V; [M-H]-
-
3-methoxybenzaldehyde Molecule
InChIKey WMPDAIZRQDCGFH-UHFFFAOYSA-N Molecular Formula C8H8O2
Related Dataset(s)
- 1H--1H correlation spectroscopy (1H-1H COSY)
- M-METHOXYBENZALDEHYDE; EI-B; MS
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- 1H--13C heteronuclear multiple bond coherence (13C-1H HMBC)
- 1H--13C heteronuclear single quantum coherence (1H-13C HSQC)
- META-METHOXYBENZALDEHYDE; EI-B; MS
-
3-methylbenzaldehyde Molecule
InChIKey OVWYEQOVUDKZNU-UHFFFAOYSA-N Molecular Formula C8H8O
Related Dataset(s)
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- correlation spectroscopy (COSY)
- heteronuclear single quantum coherence (HSQC)
- heteronuclear multiple bond coherence (HMBC)
- M-METHYLBENZALDEHYDE; EI-B; MS
- META TOLUALDEHYDE; EI-B; MS
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- distortionless enhancement with polarization transfer (DEPT)
- distortionless enhancement with polarization transfer (DEPT)
-
3-phenylpropanenitrile Molecule
InChIKey ACRWYXSKEHUQDB-UHFFFAOYSA-N Molecular Formula C9H9N
Related Dataset(s)
-
4-(2-aminoethyl)phenol Molecule
InChIKey DZGWFCGJZKJUFP-UHFFFAOYSA-N Molecular Formula C8H11NO
Related Dataset(s)
- Tyramine; LC-ESI-QTOF; MS2; CE: 10 eV; R=35000; [M+H]+
- Tyramine; LC-ESI-QTOF; MS2; HILIC; CE: 30 eV; R=35000; [M+H]+
- Tyramine; EI-B; MS; n TMS; RT: 788.72 s
- Tyramine; LC-ESI-QTOF; MS2
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- Tyramine; LC-ESI-QQ; MS2; CE:30 V; [M+H]+
- Hydroxyphenethylamine; LC-ESI-QTOF; MS2; CE:20 eV; [M+H]+
- Tyramine; LC-ESI-QTOF; MS2; HILIC; CE: 10 eV; R=35000; [M+H]+
- Tyramine; LC-ESI-QTOF; MS2; CE:30 eV; [M+H]+
- Tyramine; LC-ESI-QQ; MS2; POSITIVE; [M+H]+; CID; 10 V
- Tyramine; LC-ESI-ITFT; MS; POS
- Tyramine; LC-ESI-ITFT; MS2; m/z:308.09; POS
- Tyramine; LC-ESI-ITFT; MS2; CE 70 eV; [M+H]+
- Tyramine; LC-ESI-QTOF; MS2; HILIC; CE: 20 eV; R=35000; [M+H]+
- TYRAMINE; LC-ESI-QTOF; MS2; CE: 20eV; R=5000; [M+H]+
- Tyramine; LC-ESI-ITFT; MS2; m/z:138.09; POS
- Tyramine; LC-ESI-QQ; MS2; POSITIVE; [M+H-NH3]+; CID; 40 V
- TYRAMINE; LC-ESI-QTOF; MS2; CE: 40eV; R=5000; [M+H]+
- Tyramine; LC-ESI-QTOF; MS2; CE:Ramp 5-60 V; [M+H]+
- Tyramine; LC-ESI-ITFT; MS2; CE 45 eV; [M+H]+
- Tyramine; LC-ESI-QTOF; MS2; CE:15 eV; [M+H]+
- Tyramine; LC-ESI-QTOF; MS2; CE:15 eV; [M+H]+
- Tyramine; LC-ESI-QQ; MS2; POSITIVE; [M+H-NH3]+; CID; 30 V
- 2-(4-Hydroxyphenyl)ethylamine, Systogene, 4-(2-Aminoethyl)phenol, Tyramine, 4-Hydroxyphenethylamine, Uteramine, 4-Hydroxy-beta-phenylethylamine, Tyrosamine; LC-ESI-QQ; MS2
- Tyramine; LC-ESI-QQ; MS2; CE:10 V; [M+H]+
- Tyramine; LC-ESI-QQ; MS2; CE:40 V; [M+H]+
- Tyramine; LC-ESI-ITFT; MS2; m/z:138.09; POS
- Tyramine; LC-ESI-ITFT; MS; POS
- Tyramine; GC-EI-TOF; MS; n TMS; RT:737.844 sec
- Tyramine; LC-ESI-QTOF; MS2; CE: 30 eV; R=35000; [M+H]+
- 1H--13C heteronuclear multiple bond coherence (13C-1H HMBC)
- Tyramine; LC-ESI-QTOF; MS2; CE: 20 eV; R=35000; [M+H]+
- Hydroxyphenethylamine; LC-ESI-QTOF; MS2; CE:10 eV; [M+H]+
- Tyramine; LC-ESI-QQ; MS2; POSITIVE; [M+H]+; CID; 30 V
- 2-(4-Hydroxyphenyl)ethylamine, Systogene, 4-(2-Aminoethyl)phenol, Tyramine, 4-Hydroxyphenethylamine, Uteramine, 4-Hydroxy-beta-phenylethylamine, Tyrosamine; LC-ESI-QQ; MS2
- 2-(4-Hydroxyphenyl)ethylamine, Systogene, 4-(2-Aminoethyl)phenol, Tyramine, 4-Hydroxyphenethylamine, Uteramine, 4-Hydroxy-beta-phenylethylamine, Tyrosamine; LC-ESI-QQ; MS2
- Tyramine; LC-ESI-ITFT; MS2; m/z:121.06; POS
- Tyramine; GC-EI-TOF; MS; 3 TMS; BP:73
- Tyramine; LC-ESI-QQ; MS2; POSITIVE; [M+H]+; CID; 20 V
- Tyramine; LC-ESI-QQ; MS2; POSITIVE; [M+H]+; CID; 40 V
- Tyramine; LC-ESI-QTOF; MS2; CE:20 eV; [M+H]+
- TYRAMINE; LC-ESI-QTOF; MS2; CE: 10eV; R=5000; [M+H]+
- Tyramine; LC-ESI-QTOF; MS2; CE:10 eV; [M+H]+
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- Tyramine; LC-ESI-ITFT; MS2; CE 35 eV; [M+H]+
- Hydroxyphenethylamine; LC-ESI-QTOF; MS2; CE:40 eV; [M+H]+
- Tyramine; GC-EI-TOF; MS; 3 TMS; BP:174
- 2-(4-Hydroxyphenyl)ethylamine, 4-(2-aminoethyl)phenol, Systogene, 4-(2-Aminoethyl)phenol, Tyramine, 4-Hydroxyphenethylamine, Uteramine, 4-Hydroxy-beta-phenylethylamine, Tyrosamine; LC-ESI-QTOF; MS2
- Tyramine; LC-ESI-QTOF; MS2; CE:20 eV; [M+H]+
- Hydroxyphenethylamine; LC-ESI-QTOF; MS2; CE:30 eV; [M+H]+
- Tyramine; LC-ESI-QQ; MS2; CE:50 V; [M+H]+
- 2-(4-Hydroxyphenyl)ethylamine, Systogene, 4-(2-Aminoethyl)phenol, Tyramine, 4-Hydroxyphenethylamine, Uteramine, 4-Hydroxy-beta-phenylethylamine, Tyrosamine; LC-ESI-QQ; MS2
- Tyramine; LC-ESI-QQ; MS2; CE:20 V; [M+H]+
- Tyramine; LC-ESI-ITFT; MS2; m/z:150.06; POS
- Tyramine; LC-ESI-ITFT; MS; [M+H]+; isotope pattern
- Tyramine; LC-ESI-QQ; MS2; POSITIVE; [M+H-NH3]+; CID; 10 V
- Tyramine; LC-ESI-ITFT; MS2; m/z:121.06; POS
- Tyramine; LC-ESI-QTOF; MS2; CE:50 eV; [M+H]+
- 4-(2 AMINOETHYL)-PHENOL; EI-B; MS
- Tyramine; LC-ESI-QQ; MS2; POSITIVE; [M+H-NH3]+; CID; 20 V
- Tyramine; LC-ESI-QTOF; MS2; CE:40 eV; [M+H]+
- Hydroxyphenethylamine; LC-ESI-QTOF; MS2; CE:50 eV; [M+H]+
- 1H--1H correlation spectroscopy (1H-1H COSY)
- 1H--13C heteronuclear single quantum coherence (1H-13C HSQC)
- Tyramine; LC-ESI-ITFT; MS2; CE 55 eV; [M+H]+
- 2-(4-Hydroxyphenyl)ethylamine, Systogene, 4-(2-Aminoethyl)phenol, Tyramine, 4-Hydroxyphenethylamine, Uteramine, 4-Hydroxy-beta-phenylethylamine, Tyrosamine; LC-ESI-QQ; MS2
- Tyramine; ESI-QQ; MS; POSITIVE
- 2-(4-Hydroxyphenyl)ethylamine, Systogene, 4-(2-Aminoethyl)phenol, Tyramine, 4-Hydroxyphenethylamine, Uteramine, 4-Hydroxy-beta-phenylethylamine, Tyrosamine; LC-ESI-QQ; MS2
-
4-[(E)-4-(4-hydroxyphenyl)hex-3-en-3-yl]phenol Molecule
InChIKey RGLYKWWBQGJZGM-ISLYRVAYSA-N Molecular Formula C18H20O2
Related Dataset(s)
- Diethylstilbestrol; LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
- distortionless enhancement with polarization transfer (DEPT)
- heteronuclear single quantum coherence (HSQC)
- Diethylstilbestrol; LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
- Diethylstilbestrol; LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
- heteronuclear multiple bond coherence (HMBC)
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- Diethylstilbestrol; LC-ESI-ITFT; MS2; CE: 35; R=15000; [M+H]+
- Diethylstilbestrol; LC-ESI-ITFT; MS2; CE: 35; R=15000; [M+H]+
- Diethylstilbestrol; LC-ESI-ITFT; MS2; CE: 80; R=15000; [M+H]+
- Diethylstilbestrol; LC-ESI-ITFT; MS2; CE: 80; R=15000; [M+H]+
- correlation spectroscopy (COSY)
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- distortionless enhancement with polarization transfer (DEPT)
- Diethylstilbestrol; LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
-
4-chloro-1-oxidopyridin-1-ium Molecule
InChIKey DPJVRASYWYOFSJ-UHFFFAOYSA-N Molecular Formula C5H4ClNO
Related Dataset(s)
- mass spectrometry (MS)
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- 4-Chloropyridine 1-oxide; ESI-QTOF; MS2; CE: 20; [M-H]-
- 4-Chloropyridine 1-oxide; ESI-QTOF; MS2; CE: 20; [M+H]+
- 4-Chloropyridine 1-oxide; ESI-QTOF; MS2; CE: 10; [M+H]+
- infrared absorption spectroscopy (IR)
- 4-Chloropyridine 1-oxide; ESI-QTOF; MS2; CE: 10; [M-H]-
- mass spectrometry (MS)
- 4-Chloropyridine 1-oxide; ESI-QTOF; MS2; CE: 40; [M+H]+
-
4-chlorobenzaldehyde Molecule
InChIKey AVPYQKSLYISFPO-UHFFFAOYSA-N Molecular Formula C7H5ClO
Related Dataset(s)
- 1H--13C heteronuclear single quantum coherence (1H-13C HSQC)
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- P-CHLOROBENZALDEHYDE; EI-B; MS
- 1H--1H correlation spectroscopy (1H-1H COSY)
- distortionless enhancement with polarization transfer (DEPT)
- 1H--13C heteronuclear multiple bond coherence (13C-1H HMBC)
- distortionless enhancement with polarization transfer (DEPT)
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
-
4-formylbenzoic acid Molecule
InChIKey GOUHYARYYWKXHS-UHFFFAOYSA-N Molecular Formula C8H6O3
Related Dataset(s)
- PARA-FORMYLBENZOIC ACID; EI-B; MS
- distortionless enhancement with polarization transfer (DEPT)
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- distortionless enhancement with polarization transfer (DEPT)
- heteronuclear multiple bond coherence (HMBC)
- correlation spectroscopy (COSY)
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- 4-CARBOXLYBENZALDEHYDE; EI-B; MS
- heteronuclear single quantum coherence (HSQC)
-
4-methoxybenzaldehyde Molecule
InChIKey ZRSNZINYAWTAHE-UHFFFAOYSA-N Molecular Formula C8H8O2
Related Dataset(s)
- ANISALDEHYDE; EI-B; MS
- 1H--1H correlation spectroscopy (1H-1H COSY)
- PARA-ANISALDEHYDE; EI-B; MS
- 4-METHOXYBENZALDEHYDE; EI-B; MS
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- PARA-METHOXYBENZALDEHYDE; EI-B; MS
- 1H--13C heteronuclear single quantum coherence (1H-13C HSQC)
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- 4-METHOXYBENZALDEHYDE; EI-B; MS
- 1H--13C heteronuclear multiple bond coherence (13C-1H HMBC)
- nuclear magnetic resonance spectroscopy (NMR)
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- 1H--13C heteronuclear single quantum coherence (1H-13C HSQC)
- 1H--13C heteronuclear multiple bond coherence (13C-1H HMBC)
- 1H--1H correlation spectroscopy (1H-1H COSY)
-
4-methylbenzenesulfonamide Molecule
InChIKey LMYRWZFENFIFIT-UHFFFAOYSA-N Molecular Formula C7H9NO2S
Related Dataset(s)
- 4-Toluenesulfonamide; LC-ESI-QFT; MS2; CE: 45; R=35000; [M+H]+
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- p-Toluenesulfonamide; LC-ESI-QFT; MS2; CE: 35 NCE; R=35000; [M+H]+
- 4-Toluenesulfonamide; LC-ESI-QFT; MS2; CE: 75; R=35000; [M-H]-
- 4-Toluenesulfonamide; LC-ESI-QFT; MS2; CE: 90; R=35000; [M+H]+
- 4-Toluenesulfonamide; LC-ESI-QFT; MS2; CE: 30; R=35000; [M-H]-
- 4-Toluenesulfonamide; LC-ESI-QFT; MS2; CE: 15; R=35000; [M+H]+
- distortionless enhancement with polarization transfer (DEPT)
- p-Toluenesulfonamide; LC-ESI-QTOF; MS2; CE: 20 eV; R=35000; [M+H]+
- p-Toluenesulfonamide; LC-ESI-ITFT; MS2; CE: 35; R=15000; [M+H]+
- p-Toluenesulfonamide; LC-ESI-ITFT; MS2; CE: 80; R=15000; [M+H]+
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- PATA-TOLUENESULFONAMIDE; EI-B; MS
- 4-Toluenesulfonamide; LC-ESI-QFT; MS2; CE: 90; R=35000; [M-H]-
- distortionless enhancement with polarization transfer (DEPT)
- 4-Toluenesulfonamide; LC-ESI-QFT; MS2; CE: 15; R=35000; [M-H]-
- 4-Toluenesulfonamide; LC-ESI-QFT; MS2; CE: 120; R=35000; [M-H]-
- 1H--13C heteronuclear single quantum coherence (1H-13C HSQC)
- correlation spectroscopy (COSY)
- P-TOLUENESULFONAMIDE; EI-B; MS
- 4-Toluenesulfonamide; LC-ESI-QFT; MS2; CE: 60; R=35000; [M-H]-
- p-Toluenesulfonamide; LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
- 4-Toluenesulfonamide; LC-ESI-QFT; MS2; CE: 180; R=35000; [M-H]-
- 4-Toluenesulfonamide; LC-ESI-QFT; MS2; CE: 30; R=35000; [M+H]+
- p-Toluenesulfonamide; LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
- 4-Toluenesulfonamide; LC-ESI-QFT; MS2; CE: 150; R=35000; [M+H]+
- 4-Toluenesulfonamide; LC-ESI-QFT; MS2; CE: 120; R=35000; [M+H]+
- p-Toluenesulfonamide; LC-ESI-QTOF; MS2; CE: 10 eV; R=35000; [M+H]+
- 4-Toluenesulfonamide; LC-ESI-QFT; MS2; CE: 45; R=35000; [M-H]-
- 1H--13C heteronuclear multiple bond coherence (13C-1H HMBC)
- 4-Toluenesulfonamide; LC-ESI-QFT; MS2; CE: 180; R=35000; [M+H]+
- 4-Toluenesulfonamide; LC-ESI-QFT; MS2; CE: 150; R=35000; [M-H]-
- 4-Toluenesulfonamide; LC-ESI-QFT; MS2; CE: 60; R=35000; [M+H]+
- 4-Toluenesulfonamide; LC-ESI-QFT; MS2; CE: 75; R=35000; [M+H]+
-
4-propan-2-ylaniline Molecule
InChIKey LRTFPLFDLJYEKT-UHFFFAOYSA-N Molecular Formula C9H13N
Related Dataset(s)
- 4-Isopropylaniline; LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- 4-Isopropylaniline; LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
- 4-Isopropylaniline; LC-ESI-ITFT; MS2; CE: 75%; R=7500; [M+H]+
- 4-Isopropylaniline; LC-ESI-ITFT; MS2; CE: 90%; R=30000; [M+H]+
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- 1H--13C heteronuclear single quantum coherence (1H-13C HSQC)
- 4-Isopropylaniline; LC-ESI-QFT; MS2; CE: 35 NCE; R=35000; [M+H]+
- 1H--1H correlation spectroscopy (1H-1H COSY)
- 4-Isopropylaniline; LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
- 4-Isopropylaniline; LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
- 4-Isopropylaniline; LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
- distortionless enhancement with polarization transfer (DEPT)
- 4-Isopropylaniline; LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
- 4-Isopropylaniline; LC-ESI-QTOF; MS2; CE: Ramp 15.7-23.5 eV; R=35000; [M+H]+
- 4-Isopropylaniline; LC-ESI-ITFT; MS2; CE: 35%; R=30000; [M+H]+
- distortionless enhancement with polarization transfer (DEPT)
- 4-Isopropylaniline; LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
- 4-Isopropylaniline; LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M+H]+
- 4-Isopropylaniline; LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
- 4-Isopropylaniline; LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M+H]+
- 1H--13C heteronuclear multiple bond coherence (13C-1H HMBC)
- 4-Isopropylaniline; LC-ESI-ITFT; MS2; CE: 90%; R=7500; [M+H]+
- 4-Isopropylaniline; LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
- 4-Isopropylaniline; LC-ESI-ITFT; MS2; CE: 80; R=15000; [M+H]+
- 4-Isopropylaniline; LC-ESI-QFT; MS2; CE: 35 NCE; R=35000; [M+H]+
- 4-Isopropylaniline; LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
- 4-Isopropylaniline; LC-ESI-ITFT; MS2; CE: 35; R=15000; [M+H]+
-
4-propan-2-ylbenzaldehyde Molecule
InChIKey WTWBUQJHJGUZCY-UHFFFAOYSA-N Molecular Formula C10H12O
Related Dataset(s)
- 4-ISOPROPYLBENZALDEHYDE; EI-B; MS
- heteronuclear single quantum coherence (HSQC)
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- heteronuclear multiple bond coherence (HMBC)
- distortionless enhancement with polarization transfer (DEPT)
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- distortionless enhancement with polarization transfer (DEPT)
- correlation spectroscopy (COSY)
-
5,10-dihydrophenazine Molecule
InChIKey IVURTNNWJAPOML-UHFFFAOYSA-N Molecular Formula C12H10N2
Related Dataset(s)
- 5,10-DIHYDROPHENAZINE; EI-B; MS
- correlation spectroscopy (COSY)
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- distortionless enhancement with polarization transfer (DEPT)
- heteronuclear single quantum coherence (HSQC)
- distortionless enhancement with polarization transfer (DEPT)
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- heteronuclear multiple bond coherence (HMBC)
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
-
5,7-dimethoxychromen-2-one Molecule
InChIKey NXJCRELRQHZBQA-UHFFFAOYSA-N Molecular Formula C11H10O4
Related Dataset(s)
- 5,7-Dimethoxy-2H-chromen-2-one; ESI-QTOF; MS2; CE: 40; [M+H]+
- 5,7-Dimethoxy-2H-chromen-2-one; LC-ESI-QFT; MS2; CE: 45; R=17500; [M+H]+
- 5,7-Dimethoxy-2H-chromen-2-one; LC-ESI-QFT; MS2; CE: 75; R=17500; [M+H]+
- 5,7-Dimethoxy-2H-chromen-2-one; ESI-QTOF; MS2; CE: 20; [M+H]+
- 5,7-Dimethoxy-2H-chromen-2-one; LC-ESI-QFT; MS2; CE: 90; R=17500; [M+H]+
- 5,7-Dimethoxy-2H-chromen-2-one; LC-ESI-QFT; MS2; CE: 60; R=17500; [M+H]+
- infrared absorption spectroscopy (IR)
- 5,7-Dimethoxy-2H-chromen-2-one; ESI-QTOF; MS2; CE: 10; [M+H]+
- 5,7-Dimethoxy-2H-chromen-2-one; LC-ESI-QFT; MS2; CE: 15; R=17500; [M+H]+
- 5,7-Dimethoxy-2H-chromen-2-one; LC-ESI-QFT; MS2; CE: 30; R=17500; [M+H]+
-
N,N'-dimethylcarbamimidothioic acid Molecule
InChIKey VLCDUOXHFNUCKK-UHFFFAOYSA-N Molecular Formula C3H8N2S
Related Dataset(s)
-
N,N-dimethyl-1-oxidopyridin-1-ium-4-amine Molecule
InChIKey WZMNQOYCHMGCSS-UHFFFAOYSA-N Molecular Formula C7H10N2O
Related Dataset(s)
-
N-(2-methylphenyl)acetamide Molecule
InChIKey BPEXTIMJLDWDTL-UHFFFAOYSA-N Molecular Formula C9H11NO
Related Dataset(s)
-
N-(4-bromophenyl)acetamide Molecule
InChIKey MSLICLMCQYQNPK-UHFFFAOYSA-N Molecular Formula C8H8BrNO
Related Dataset(s)
- electron ionisation mass spectrometry (EI-MS)
- infrared absorption spectroscopy (IR)
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- mass spectrometry (MS)
- 4`-Bromacetanilide; LC-ESI-QFT; MS2; CE: 35 NCE; R=35000; [M+H]+
- infrared absorption spectroscopy (IR)
- 4`-Bromacetanilide; LC-ESI-QFT; MS2; CE: 35 NCE; R=35000; [M-H]-
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
-
N-benzyl-1-phenylmethanamine Molecule
InChIKey BWLUMTFWVZZZND-UHFFFAOYSA-N Molecular Formula C14H15N
Related Dataset(s)
- Dibenzylamine; LC-ESI-QTOF; MS2; 130 V
- Dibenzylamine; LC-ESI-QTOF; MS2; 20 V
- Dibenzylamine; LC-ESI-QTOF; MS2; 30 V
- Dibenzylamine; LC-ESI-QTOF; MS2; 140 V
- Dibenzylamine; LC-ESI-QTOF; MS2; 150 V
- DIBENZYLAMINE; EI-B; MS
- Dibenzylamine; LC-ESI-QTOF; MS2; 120 V
- Dibenzylamine; LC-ESI-QTOF; MS2; 100 V
- electron ionisation mass spectrometry (EI-MS)
- Dibenzylamine; LC-ESI-QTOF; MS2; 80 V
- Dibenzylamine; LC-ESI-QTOF; MS2; 40 V
- infrared absorption spectroscopy (IR)
- Dibenzylamine; LC-ESI-QTOF; MS2; 90 V
- Dibenzylamine; LC-ESI-QTOF; MS2; 40 V
- Dibenzylamine; LC-ESI-QTOF; MS2; 10 V
- Dibenzylamine; LC-ESI-QTOF; MS2; 50 V
- Dibenzylamine; LC-ESI-QTOF; MS2; 110 V
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- Dibenzylamine; LC-ESI-QTOF; MS2; 70 V
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- Dibenzylamine; LC-ESI-QTOF; MS2; 60 V
