ACCESSION: MSBNK-RIKEN_ReSpect-PT211430
RECORD_TITLE: (E)-3-(4-hydroxyphenyl)prop-2-enoic acid, trans-4-Hydroxycinnamic acid, p-Coumaric acid; LC-ESI-QTOF; MS2
DATE: 2008.07.29
AUTHORS: Matsuda F, Suzuki M, Sawada Y, Plant Science Center, RIKEN.
LICENSE: CC BY-NC
COPYRIGHT: Copyright(C) 2009 Plant Science Center, RIKEN
COMMENT: Build 1 2009/06/24
COMMENT: Acquisition and generation of the data is financially supported in part by CREST/JST.

CH$NAME: (E)-3-(4-hydroxyphenyl)prop-2-enoic acid
CH$NAME: trans-4-Hydroxycinnamic acid
CH$NAME: p-Coumaric acid
CH$COMPOUND_CLASS: CLASS1 Phenylpropanoid CLASS2 Phenylpropanoid monomer CLASS3 p-Coumaric acid
CH$FORMULA: C₉H₈O₃
CH$EXACT_MASS: 164.16
CH$SMILES: C1=CC(=CC=C1C=CC(=O)O)O
CH$IUPAC: InChI=1S/C9H8O3/c10-8-4-1-7(2-5-8)3-6-9(11)12/h1-6,10H,(H,11,12)
CH$LINK: CAS 501-98-4
CH$LINK: INCHIKEY NGSWKAQJJWESNS-UHFFFAOYSA-N

AC$INSTRUMENT: Q-Tof Premier, Waters
AC$INSTRUMENT_TYPE: LC-ESI-QTOF
AC$MASS_SPECTROMETRY: MS_TYPE MS2
AC$MASS_SPECTROMETRY: ION_MODE NEGATIVE
AC$MASS_SPECTROMETRY: IONIZATION ESI
AC$MASS_SPECTROMETRY: COLLISION_ENERGY Ramp 5-45 V
AC$MASS_SPECTROMETRY: CAPILLARY_VOLTAGE 3.0 kV
AC$CHROMATOGRAPHY: SOLVENT CH3CN/H2O

MS$FOCUSED_ION: ION_TYPE [M-H]-
MS$FOCUSED_ION: PRECURSOR_M/Z 163.03954

PK$SPLASH: splash10-03di-0900000000-fbb6439b7d012045f3a8
PK$NUM_PEAK: 5
PK$PEAK: m/z int. rel.int.
  101.0121 4.298 10
  118.9791 4.32 10
  145.8717 196.0 472
  162.8717 415.0 999
  163.0395 5.227 13
//