ACCESSION: MSBNK-Keio_Univ-KO000442
RECORD_TITLE: 2-Coumaric acid; LC-ESI-QQ; MS2; CE:20 V; [M-H]-
DATE: 2016.01.19 (Created 2007.07.07, modified 2011.05.10)
AUTHORS: Kakazu Y, Horai H, Institute for Advanced Biosciences, Keio Univ.
LICENSE: CC BY-NC-SA
COMMENT: KEIO_ID C039

CH$NAME: o-Coumarate
CH$NAME: trans-2-Hydroxycinnamate
CH$NAME: trans-2-Hydroxycinnamic acid
CH$NAME: 2-Coumaric acid
CH$COMPOUND_CLASS: N/A
CH$FORMULA: C₉H₈O₃
CH$EXACT_MASS: 164.04734
CH$SMILES: OC(=O)C=Cc(c1)c(O)ccc1
CH$IUPAC: InChI=1S/C9H8O3/c10-8-4-2-1-3-7(8)5-6-9(11)12/h1-6,10H,(H,11,12)/b6-5+
CH$LINK: CAS 614-60-8
CH$LINK: CHEBI 18125
CH$LINK: KEGG C01772
CH$LINK: NIKKAJI J55.415D
CH$LINK: PUBCHEM SID:4905
CH$LINK: INCHIKEY PMOWTIHVNWZYFI-AATRIKPKSA-N
CH$LINK: COMPTOX DTXSID10883240

AC$INSTRUMENT: API3000, Applied Biosystems
AC$INSTRUMENT_TYPE: LC-ESI-QQ
AC$MASS_SPECTROMETRY: MS_TYPE MS2
AC$MASS_SPECTROMETRY: ION_MODE NEGATIVE
AC$MASS_SPECTROMETRY: COLLISION_ENERGY 20 V

MS$FOCUSED_ION: PRECURSOR_M/Z 163
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-

PK$SPLASH: splash10-014i-0900000000-efd5de4e7fe4032816f6
PK$NUM_PEAK: 10
PK$PEAK: m/z int. rel.int.
  59.200 49505.0 1
  91.100 29703.0 1
  93.300 108911.0 2
  106.800 64356.5 1
  116.900 321782.5 7
  118.500 881189.0 19
  119.000 46316878.0 999
  128.200 19802.0 1
  135.300 94059.5 2
  163.200 1222773.5 26
//