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1-fluoro-2-phenylbenzene Molecule
InChIKey KLECYOQFQXJYBC-UHFFFAOYSA-N Molecular Formula C12H9F
Related Dataset(s)
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2-iodo-N-phenylbenzamide Molecule
InChIKey LJOZMWRYMKECFF-UHFFFAOYSA-N Molecular Formula C13H10INO
Related Dataset(s)
- infrared absorption spectroscopy (IR)
- Benodanil; LC-ESI-QFT; MS2; CE: 15; R=17500; [M+H]+
- Benodanil; LC-ESI-QFT; MS2; CE: 15%; R=17500; [M+H]+
- Benodanil; LC-ESI-QTOF; MS2; 20 V
- Benodanil; LC-ESI-QTOF; MS2; 110 V
- Benodanil; LC-ESI-QFT; MS2; CE: 45%; R=17500; [M+H]+
- Benodanil; LC-ESI-QTOF; MS2; 140 V
- Benodanil; LC-ESI-QTOF; MS2; 80 V
- Benodanil; LC-ESI-QTOF; MS2; 90 V
- Benodanil; LC-ESI-QTOF; MS2; 10 V
- Benodanil; LC-ESI-QTOF; MS2; 60 V
- Benodanil; LC-ESI-QTOF; MS2; 50 V
- Benodanil; LC-ESI-QTOF; MS2; 120 V
- Benodanil; LC-ESI-QTOF; MS2; 120 V
- Benodanil; LC-ESI-QTOF; MS2; 150 V
- Benodanil; LC-ESI-QFT; MS2; CE: 120%; R=17500; [M+H]+
- Benodanil; LC-ESI-QFT; MS2; CE: 150%; R=17500; [M+H]+
- Benodanil; LC-ESI-QTOF; MS2; 70 V
- Benodanil; LC-ESI-QTOF; MS2; 40 V
- Benodanil; LC-ESI-QTOF; MS2; 40 V
- Benodanil; LC-ESI-QFT; MS2; CE: 75; R=17500; [M+H]+
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- Benodanil; LC-ESI-QTOF; MS2; 130 V
- Benodanil; LC-ESI-QTOF; MS2; 50 V
- Benodanil; LC-ESI-QFT; MS2; CE: 60%; R=17500; [M+H]+
- Benodanil; LC-ESI-QFT; MS2; CE: 30; R=17500; [M+H]+
- Benodanil; LC-ESI-QTOF; MS2; 40 V
- Benodanil; LC-ESI-QTOF; MS2; 130 V
- Benodanil; LC-ESI-QTOF; MS2; 40 V
- Benodanil; LC-ESI-QTOF; MS2; 150 V
- Benodanil; LC-ESI-QTOF; MS2; 80 V
- Benodanil; LC-ESI-QFT; MS2; CE: 180%; R=17500; [M+H]+
- Benodanil; LC-ESI-QFT; MS2; CE: 90; R=17500; [M+H]+
- Benodanil; LC-ESI-QTOF; MS2; 30 V
- Benodanil; LC-ESI-QTOF; MS2; 100 V
- Benodanil; LC-ESI-QTOF; MS2; 60 V
- Benodanil; LC-ESI-QFT; MS2; CE: 30%; R=17500; [M+H]+
- Benodanil; LC-ESI-QTOF; MS2; 20 V
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- Benodanil; LC-ESI-QTOF; MS2; 110 V
- Benodanil; LC-ESI-QTOF; MS2; 90 V
- Benodanil; LC-ESI-QFT; MS2; CE: 45; R=17500; [M+H]+
- Benodanil; LC-ESI-QTOF; MS2; 100 V
- electron ionisation mass spectrometry (EI-MS)
- Benodanil; LC-ESI-QTOF; MS2; 30 V
- Benodanil; LC-ESI-QFT; MS2; CE: 60; R=17500; [M+H]+
- Benodanil; LC-ESI-QFT; MS2; CE: 75%; R=17500; [M+H]+
- Benodanil; LC-ESI-QTOF; MS2; 140 V
- Benodanil; LC-ESI-QTOF; MS2; 10 V
- Benodanil; LC-ESI-QTOF; MS2; 70 V
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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)
- infrared absorption spectroscopy (IR)
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- mass spectrometry (MS)
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- 4`-Bromacetanilide; LC-ESI-QFT; MS2; CE: 35 NCE; R=35000; [M-H]-
- 4`-Bromacetanilide; LC-ESI-QFT; MS2; CE: 35 NCE; R=35000; [M+H]+
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N-benzyl-1-phenylmethanamine Molecule
InChIKey BWLUMTFWVZZZND-UHFFFAOYSA-N Molecular Formula C14H15N
Related Dataset(s)
- Dibenzylamine; LC-ESI-QTOF; MS2; 150 V
- Dibenzylamine; LC-ESI-QTOF; MS2; 100 V
- electron ionisation mass spectrometry (EI-MS)
- Dibenzylamine; LC-ESI-QTOF; MS2; 40 V
- Dibenzylamine; LC-ESI-QTOF; MS2; 40 V
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- Dibenzylamine; LC-ESI-QTOF; MS2; 60 V
- Dibenzylamine; LC-ESI-QTOF; MS2; 130 V
- Dibenzylamine; LC-ESI-QTOF; MS2; 70 V
- Dibenzylamine; LC-ESI-QTOF; MS2; 30 V
- Dibenzylamine; LC-ESI-QTOF; MS2; 90 V
- Dibenzylamine; LC-ESI-QTOF; MS2; 140 V
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- Dibenzylamine; LC-ESI-QTOF; MS2; 20 V
- DIBENZYLAMINE; EI-B; MS
- Dibenzylamine; LC-ESI-QTOF; MS2; 110 V
- Dibenzylamine; LC-ESI-QTOF; MS2; 10 V
- infrared absorption spectroscopy (IR)
- Dibenzylamine; LC-ESI-QTOF; MS2; 120 V
- Dibenzylamine; LC-ESI-QTOF; MS2; 50 V
- Dibenzylamine; LC-ESI-QTOF; MS2; 80 V
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N-benzylprop-2-yn-1-amine Molecule
InChIKey LDYBFSGEBHSTOQ-UHFFFAOYSA-N Molecular Formula C10H11N
Related Dataset(s)
- Raman spectroscopy (Raman spectrometry)
- PAR_146.0966_8.3; LC-ESI-QFT; MS2; CE: 30; R=17500; [M+H]+
- PAR_146.0966_8.3; LC-ESI-QFT; MS2; CE: 90; R=17500; [M+H]+
- PAR_146.0966_8.3; LC-ESI-QFT; MS2; CE: 45; R=17500; [M+H]+
- PAR_146.0966_8.3; LC-ESI-QFT; MS2; CE: 75; R=17500; [M+H]+
- thin-layer chromatography (TLC)
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- PAR_146.0966_8.3; LC-ESI-QFT; MS2; CE: 15; R=17500; [M+H]+
- infrared absorption spectroscopy (IR)
- PAR_146.0966_8.3; LC-ESI-QFT; MS2; CE: 60; R=17500; [M+H]+
- electron ionisation mass spectrometry (EI-MS)
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[4-(sulfanylmethyl)phenyl]methanethiol Molecule
InChIKey IYPNRTQAOXLCQW-UHFFFAOYSA-N Molecular Formula C8H10S2
Related Dataset(s)
- thin-layer chromatography (TLC)
- correlation spectroscopy (COSY)
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- heteronuclear single quantum coherence (HSQC)
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- infrared absorption spectroscopy (IR)
- electron ionisation mass spectrometry (EI-MS)
- infrared absorption spectroscopy (IR)
- electron ionisation mass spectrometry (EI-MS)
- 13C nuclear magnetic resonance spectroscopy (13C NMR)
- distortionless enhancement with polarization transfer (DEPT)
- infrared absorption spectroscopy (IR)
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- 1H nuclear magnetic resonance spectroscopy (1H NMR)
- fast-atom bombardment mass spectrometry (FABMS)
- distortionless enhancement with polarization transfer (DEPT)
- 1,4-BIS(MERCAPTOMETHYL)BENZENE; EI-B; MS
