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1-(4-phenylphenyl)ethanone Molecule
InChIKey QCZZSANNLWPGEA-UHFFFAOYSA-N Molecular Formula C14H12O
Related Dataset(s)
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1-oxidopyridin-1-ium Molecule
InChIKey ILVXOBCQQYKLDS-UHFFFAOYSA-N Molecular Formula C5H5NO
Related Dataset(s)
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1H-quinolin-2-one Molecule
InChIKey LISFMEBWQUVKPJ-UHFFFAOYSA-N Molecular Formula C9H7NO
Related Dataset(s)
- 2-Hydroxyquinoline; LC-ESI-QTOF; MS2; CE: 30 eV; R=35000; [M+H]+
- infrared absorption spectroscopy (IR)
- 2-Hydroxyquinoline; LC-ESI-ITFT; MS2; CE: 10%; R=15000; [M+H]+
- 2-Hydroxyquinoline; LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- 2-Hydroxyquinoline; LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- 2-Hydroxyquinoline; LC-ESI-QTOF; MS2; CE: 10 eV; R=35000; [M+H]+
- 2-Hydroxyquinoline; LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
- distortionless enhancement with polarization transfer (DEPT)
- 2-Hydroxyquinoline; LC-ESI-QTOF; MS2; CE: Ramp 16.1-24.1 eV; R=35000; [M+H]+
- distortionless enhancement with polarization transfer (DEPT)
- 2-Hydroxyquinoline; LC-ESI-QTOF; MS2; CE: 50 eV; R=35000; [M+H]+
- 2(1H)-Quinolinone; LC-ESI-QQ; MS2; CE:40 V; [M+H]+
- 2-Hydroxyquinoline; LC-ESI-QTOF; MS2; CE: 40 eV; R=35000; [M+H]+
- 2-Hydroxyquinoline; LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
- 2(1H)-Quinolinone; LC-ESI-QQ; MS2; CE:50 V; [M+H]+
- 2(1H)-Quinolinone; LC-ESI-QQ; MS2; CE:20 V; [M+H]+
- 2(1H)-Quinolinone; LC-ESI-QQ; MS2; CE:30 V; [M+H]+
- 2-Hydroxyquinoline; LC-ESI-QFT; MS2; CE: 50%; R=35000; [M+H]+
- 2-Hydroxyquinoline; LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
- 2-Hydroxyquinoline; LC-ESI-QTOF; MS2; CE: 20 eV; R=35000; [M+H]+
- mass spectrometry (MS)
- 2-Hydroxyquinoline; LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
- 2-Hydroxyquinoline; LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
- 2-Hydroxyquinoline; LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
- 2(1H)-Quinolinone; LC-ESI-QQ; MS2; CE:10 V; [M+H]+
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4-chloro-1-oxidopyridin-1-ium Molecule
InChIKey DPJVRASYWYOFSJ-UHFFFAOYSA-N Molecular Formula C5H4ClNO
Related Dataset(s)
- 4-Chloropyridine 1-oxide; ESI-QTOF; MS2; CE: 10; [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: 40; [M+H]+
- 4-Chloropyridine 1-oxide; ESI-QTOF; MS2; CE: 20; [M-H]-
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- mass spectrometry (MS)
- 4-Chloropyridine 1-oxide; ESI-QTOF; MS2; CE: 20; [M+H]+
- mass spectrometry (MS)
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N-(2-methylphenyl)acetamide Molecule
InChIKey BPEXTIMJLDWDTL-UHFFFAOYSA-N Molecular Formula C9H11NO
Related Dataset(s)
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N-(4-bromophenyl)acetamide Molecule
InChIKey MSLICLMCQYQNPK-UHFFFAOYSA-N Molecular Formula C8H8BrNO
Related Dataset(s)
- infrared absorption spectroscopy (IR)
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- 4`-Bromacetanilide; LC-ESI-QFT; MS2; CE: 35 NCE; R=35000; [M+H]+
- infrared absorption spectroscopy (IR)
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- 4`-Bromacetanilide; LC-ESI-QFT; MS2; CE: 35 NCE; R=35000; [M-H]-
- electron ionisation mass spectrometry (EI-MS)
- mass spectrometry (MS)
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
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diethyl benzene-1,4-dicarboxylate Molecule
InChIKey ONIHPYYWNBVMID-UHFFFAOYSA-N Molecular Formula C12H14O4
Related Dataset(s)
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ethyl 4-acetamidobenzoate Molecule
InChIKey NHLOBHNRBWKNIO-UHFFFAOYSA-N Molecular Formula C11H13NO3
Related Dataset(s)
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phenylphosphonic acid Molecule
InChIKey QLZHNIAADXEJJP-UHFFFAOYSA-N Molecular Formula C6H7O3P
Related Dataset(s)
- Phenylphosphonic Acid; LC-ESI-QFT; MS2; CE: 60%; R=15000; [M-H]-
- infrared absorption spectroscopy (IR)
- Phenylphosphonic acid; LC-ESI-QTOF; MS2; 60 V
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- Phenylphosphonic acid; LC-ESI-QTOF; MS2; 150 V
- Phenylphosphonic Acid; LC-ESI-QFT; MS2; CE: 75%; R=15000; [M-H]-
- Phenylphosphonic Acid; LC-ESI-QFT; MS2; CE: 45%; R=15000; [M+H]+
- Phenylphosphonic acid; LC-ESI-QTOF; MS2; 120 V
- Phenylphosphonic Acid; LC-ESI-QFT; MS2; CE: 180%; R=15000; [M+H]+
- Phenylphosphonic acid; ESI-QTOF; MS2; CE: 40; [M-H]-
- Phenylphosphonic acid; LC-ESI-QTOF; MS2; 60 V
- Phenylphosphonic acid; LC-ESI-QTOF; MS2; 50 V
- Phenylphosphonic Acid; LC-ESI-QFT; MS2; CE: 120%; R=15000; [M+H]+
- Phenylphosphonic acid; LC-ESI-QTOF; MS2; 20 V
- Phenylphosphonic acid; LC-ESI-QTOF; MS2; 20 V
- Phenylphosphonic Acid; LC-ESI-QFT; MS2; CE: 120%; R=15000; [M-H]-
- Phenylphosphonic Acid; LC-ESI-QFT; MS2; CE: 150%; R=15000; [M-H]-
- Phenylphosphonic acid; LC-ESI-QTOF; MS2; 30 V
- Phenylphosphonic acid; ESI-QTOF; MS2; CE: 20; [M-H]-
- Phenylphosphonic acid; LC-ESI-QTOF; MS2; 90 V
- Phenylphosphonic acid; LC-ESI-QTOF; MS2; 100 V
- Phenylphosphonic Acid; LC-ESI-QFT; MS2; CE: 15%; R=15000; [M-H]-
- Phenylphosphonic Acid; LC-ESI-QFT; MS2; CE: 150%; R=15000; [M+H]+
- Phenylphosphonic acid; LC-ESI-QTOF; MS2; 40 V
- Phenylphosphonic acid; LC-ESI-QTOF; MS2; 140 V
- Phenylphosphonic Acid; LC-ESI-QFT; MS2; CE: 90%; R=15000; [M-H]-
- distortionless enhancement with polarization transfer (DEPT)
- PHENYLPHOSPHONIC ACID; EI-B; MS
- Phenylphosphonic acid; LC-ESI-QTOF; MS2; 10 V
- Phenylphosphonic acid; ESI-QTOF; MS2; CE: 10; [M-H]-
- Phenylphosphonic Acid; LC-ESI-QFT; MS2; CE: 180%; R=15000; [M-H]-
- Phenylphosphonic Acid; LC-ESI-QFT; MS2; CE: 75%; R=15000; [M+H]+
- Phenylphosphonic acid; LC-ESI-QTOF; MS2; 130 V
- Phenylphosphonic Acid; LC-ESI-QFT; MS2; CE: 30%; R=15000; [M+H]+
- Phenylphosphonic Acid; LC-ESI-QFT; MS2; CE: 90%; R=15000; [M+H]+
- 31P nuclear magnetic resonance spectroscopy (31P NMR)
- Phenylphosphonic Acid; LC-ESI-QFT; MS2; CE: 15%; R=15000; [M+H]+
- Phenylphosphonic Acid; LC-ESI-QFT; MS2; CE: 60%; R=15000; [M+H]+
- mass spectrometry (MS)
- Phenylphosphonic acid; LC-ESI-QTOF; MS2; 110 V
- Phenylphosphonic acid; LC-ESI-QTOF; MS2; 30 V
- Phenylphosphonic acid; LC-ESI-QTOF; MS2; 40 V
- Phenylphosphonic acid; LC-ESI-QTOF; MS2; 40 V
- Phenylphosphonic acid; LC-ESI-QTOF; MS2; 10 V
- Phenylphosphonic Acid; LC-ESI-QFT; MS2; CE: 45%; R=15000; [M-H]-
- Phenylphosphonic acid; LC-ESI-QTOF; MS2; 70 V
- Phenylphosphonic acid; LC-ESI-QTOF; MS2; 40 V
- Phenylphosphonic acid; LC-ESI-QTOF; MS2; 80 V
- Phenylphosphonic Acid; LC-ESI-QFT; MS2; CE: 30%; R=15000; [M-H]-
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quinoxaline Molecule
InChIKey XSCHRSMBECNVNS-UHFFFAOYSA-N Molecular Formula C8H6N2
Related Dataset(s)
- Quinoxaline; LC-ESI-QFT; MS2; CE: 35 NCE; R=35000; [M+H]+
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- mass spectrometry (MS)
- QUINOXALINE; EI-B; MS
- elemental analysis (EA)
- mass spectrometry (MS)
- infrared absorption spectroscopy (IR)
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- QUINOXALINE; EI-B; MS
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- infrared absorption spectroscopy (IR)
