ACCESSION: MSBNK-LCSB-LU136656
RECORD_TITLE: Leflunomide; LC-ESI-QFT; MS2; CE: 90; R=17500; [M-H]-
DATE: 2020.08.19
AUTHORS: Elapavalore, A.; Kondić, T.; Singh, R.; Schymanski, E.
LICENSE: CC BY
COPYRIGHT: Copyright © 2019 by Environmental Cheminformatics, LCSB, University of Luxembourg, Luxembourg
PUBLICATION: Elapavalore, A.; Kondić, T.; et al., Adding Open Spectral Data to MassBank and PubChem Using Open Source Tools to Support Non-Targeted Exposomics of Mixtures (submitted).
PROJECT: ENTACT U.S. Environmental Protection Agency’s Non-Targeted Analysis Collaborative Trial
COMMENT: CONFIDENCE standard compound
COMMENT: INTERNAL_ID 1366
COMMENT: DATASET 20200303_ENTACT_RP_MIX507
COMMENT: DATA_PROCESSING MERGING RMBmix ver. 0.2.7
COMMENT: DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0
COMMENT: ORIGINAL_ACQUISITION_NO 4423
COMMENT: ORIGINAL_PRECURSOR_SCAN_NO 4422
COMMENT: RAW_DATA available as MSV000091754 at [DOI:10.25345/C5S46HG75]

CH$NAME: Leflunomide
CH$NAME: 5-methyl-N-[4-(trifluoromethyl)phenyl]-1,2-oxazole-4-carboxamide
CH$COMPOUND_CLASS: N/A; Environmental Standard
CH$FORMULA: C₁₂H₉F₃N₂O₂
CH$EXACT_MASS: 270.0616
CH$SMILES: CC1=C(C=NO1)C(=O)NC1=CC=C(C=C1)C(F)(F)F
CH$IUPAC: InChI=1S/C12H9F3N2O2/c1-7-10(6-16-19-7)11(18)17-9-4-2-8(3-5-9)12(13,14)15/h2-6H,1H3,(H,17,18)
CH$LINK: CAS 75706-12-6
CH$LINK: CHEBI 6402
CH$LINK: KEGG C07905
CH$LINK: PUBCHEM CID:3899
CH$LINK: INCHIKEY VHOGYURTWQBHIL-UHFFFAOYSA-N
CH$LINK: CHEMSPIDER 3762

AC$INSTRUMENT: Q Exactive Orbitrap (Thermo Scientific)
AC$INSTRUMENT_TYPE: LC-ESI-QFT
AC$MASS_SPECTROMETRY: MS_TYPE MS2
AC$MASS_SPECTROMETRY: ION_MODE NEGATIVE
AC$MASS_SPECTROMETRY: IONIZATION ESI
AC$MASS_SPECTROMETRY: FRAGMENTATION_MODE HCD
AC$MASS_SPECTROMETRY: COLLISION_ENERGY 90
AC$MASS_SPECTROMETRY: RESOLUTION 17500
AC$CHROMATOGRAPHY: COLUMN_NAME Acquity BEH C18 1.7um, 2.1x150mm (Waters)
AC$CHROMATOGRAPHY: FLOW_GRADIENT 90/10 at 0-2 min, 0/100 at 15-20 min, 90/10 at 20.1-30 min
AC$CHROMATOGRAPHY: FLOW_RATE 0.20 mL/min
AC$CHROMATOGRAPHY: RETENTION_TIME 17.644 min
AC$CHROMATOGRAPHY: SOLVENT A 0.1% formic acid
AC$CHROMATOGRAPHY: SOLVENT B methanol

MS$FOCUSED_ION: BASE_PEAK 269.0543
MS$FOCUSED_ION: PRECURSOR_M/Z 269.0543
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$FOCUSED_ION: PRECURSOR_INTENSITY 133019269.2207
MS$DATA_PROCESSING: RECALIBRATE loess on assigned fragments and MS1
MS$DATA_PROCESSING: REANALYZE Peaks with additional N2/O included
MS$DATA_PROCESSING: WHOLE RMassBank 2.99.2

PK$SPLASH: splash10-00lr-9200000000-17bb1c1f9a5407acb882
PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm)
  64.0193 C4H2N- 1 64.0193 -0.03
  65.0033 C4HO- 1 65.0033 0.29
  65.0146 C3HN2- 1 65.0145 1.42
  65.9985 C3NO- 1 65.9985 0.1
  74.0036 C5N- 1 74.0036 0.19
  82.0298 C4H4NO- 2 82.0298 0.04
  83.0142 C4H3O2- 1 83.0139 4.53
  100.0194 C7H2N- 2 100.0193 0.77
  107.0254 C5H3N2O- 2 107.0251 2.94
  117.0346 C8H5O- 2 117.0346 -0.24
  120.0255 C7H3FN- 2 120.0255 -0.03
  138.0361 C7H5FNO- 3 138.0361 0.15
  140.0317 C7H4F2N- 2 140.0317 -0.47
  145.021 C8H2FN2- 3 145.0207 1.95
  160.038 C7H5F3N- 1 160.038 0.26
PK$NUM_PEAK: 15
PK$PEAK: m/z int. rel.int.
  64.0193 507792.7 101
  65.0033 7381.4 1
  65.0146 36338 7
  65.9985 3033901.2 607
  74.0036 92676.9 18
  82.0298 4985939.5 999
  83.0142 8552.4 1
  100.0194 824398.4 165
  107.0254 7228.7 1
  117.0346 38702.5 7
  120.0255 472706.4 94
  138.0361 109036.6 21
  140.0317 74748.6 14
  145.021 26728.8 5
  160.038 507362.9 101
//