MassBank Record: AU203101



 Azoxystrobin acid; LC-ESI-QTOF; MS2; CE: 10 eV; R=35000; [M+H]+ 
Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk) \n

ACCESSION: AU203101
RECORD_TITLE: Azoxystrobin acid; LC-ESI-QTOF; MS2; CE: 10 eV; R=35000; [M+H]+
DATE: 2015.12.03
AUTHORS: , Nikiforos Alygizakis, Nikolaos Thomaidis, University of Athens
LICENSE: CC BY-SA
COPYRIGHT: Copyright (C) 2015 Department of Chemistry, University of Athens
COMMENT: CONFIDENCE standard compound
COMMENT: INTERNAL_ID 2031

CH$NAME: Azoxystrobin acid CH$NAME: SCHEMBL435486 CH$NAME: (E)-2-[2-[6-(2-cyanophenoxy)pyrimidin-4-yl]oxyphenyl]-3-methoxyprop-2-enoic acid CH$COMPOUND_CLASS: N/A; Environmental Standard CH$FORMULA: C21H15N3O5 CH$EXACT_MASS: 389.1011706 CH$SMILES: CO\C=C(\C(O)=O)c1ccccc1Oc1cc(Oc2ccccc2C#N)ncn1 CH$IUPAC: InChI=1S/C21H15N3O5/c1-27-12-16(21(25)26)15-7-3-5-9-18(15)29-20-10-19(23-13-24-20)28-17-8-4-2-6-14(17)11-22/h2-10,12-13H,1H3,(H,25,26)/b16-12+ CH$LINK: CAS 1185255-09-7 CH$LINK: CHEBI 83496 CH$LINK: PUBCHEM CID:66685656 CH$LINK: INCHIKEY IKCXDZCEWZARFL-FOWTUZBSSA-N CH$LINK: CHEMSPIDER 28184900 CH$LINK: COMPTOX DTXSID10891507
AC$INSTRUMENT: Bruker maXis Impact AC$INSTRUMENT_TYPE: LC-ESI-QTOF AC$MASS_SPECTROMETRY: MS_TYPE MS2 AC$MASS_SPECTROMETRY: ION_MODE POSITIVE AC$MASS_SPECTROMETRY: IONIZATION ESI AC$MASS_SPECTROMETRY: FRAGMENTATION_MODE CID AC$MASS_SPECTROMETRY: COLLISION_ENERGY 10 eV AC$MASS_SPECTROMETRY: RESOLUTION 35000 AC$CHROMATOGRAPHY: COLUMN_NAME Acclaim RSLC C18 2.2um, 2.1x100mm, Thermo AC$CHROMATOGRAPHY: FLOW_GRADIENT 99/1 at 0-1 min, 61/39 at 3 min, 0.1/99.9 at 14-16 min, 99/1 at 16.1-20 min AC$CHROMATOGRAPHY: FLOW_RATE 200 uL/min at 0-3 min, 400 uL/min at 14 min, 480 uL/min at 16-19 min, 200 uL/min at 19.1-20 min AC$CHROMATOGRAPHY: RETENTION_TIME 8.0 min AC$CHROMATOGRAPHY: SOLVENT A 90:10 water:methanol with 0.01% formic acid and 5mM ammonium formate AC$CHROMATOGRAPHY: SOLVENT B methanol with 0.01% formic acid and 5mM ammonium formate
MS$FOCUSED_ION: BASE_PEAK 390.1083 MS$FOCUSED_ION: PRECURSOR_M/Z 390.1084 MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+ MS$DATA_PROCESSING: RECALIBRATE identity on assigned fragments and MS1 MS$DATA_PROCESSING: REANALYZE Peaks with additional N2/O included MS$DATA_PROCESSING: WHOLE RMassBank 2.0.3
PK$SPLASH: splash10-00di-0009000000-00b72673b435e31ee396 PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm) 149.0225 C6H3N3O2+ 2 149.022 3.66 344.104 C20H14N3O3+ 1 344.103 3.04 346.1181 C20H16N3O3+ 1 346.1186 -1.48 372.0981 C21H14N3O4+ 1 372.0979 0.55 373.1009 C20[13]CH14N3O4+ 1 373.1018 -2.35 374.1024 C19[13]C2H14N3O4+ 2 374.1036 -6.94 390.1086 C21H16N3O5+ 1 390.1084 0.49 391.1116 C20[13]CH16N3O5+ 1 391.1115 0.26 392.1142 C19[13]C2H16N3O5+ 1 392.1141 0.26 PK$NUM_PEAK: 9 PK$PEAK: m/z int. rel.int. 149.0225 1132 6 344.104 992 5 346.1181 2220 12 372.0981 173636 999 373.1009 39484 227 374.1024 4712 27 390.1086 79496 457 391.1116 18312 105 392.1142 2192 13 //

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