ACCESSION: MSBNK-Fac_Eng_Univ_Tokyo-JP004072
RECORD_TITLE: OXAZEPAM; EI-B; MS
DATE: 2016.01.19 (Created 2008.10.21, modified 2011.05.06)
AUTHORS: YAMAMOTO M, DEP. CHEMISTRY, FAC. SCIENCE, NARA WOMEN'S UNIV.
LICENSE: CC BY-NC-SA

CH$NAME: OXAZEPAM
CH$COMPOUND_CLASS: N/A
CH$FORMULA: C₁₅H₁₁ClN₂O₂
CH$EXACT_MASS: 286.05091
CH$SMILES: Clc(c3)cc(c(c3)2)C(=NC(O)C(=O)N2)c(c1)cccc1
CH$IUPAC: InChI=1S/C15H11ClN2O2/c16-10-6-7-12-11(8-10)13(9-4-2-1-3-5-9)18-15(20)14(19)17-12/h1-8,15,20H,(H,17,19)
CH$LINK: INCHIKEY ADIMAYPTOBDMTL-UHFFFAOYSA-N
CH$LINK: COMPTOX DTXSID1021087

AC$INSTRUMENT: HITACHI RMU-6E
AC$INSTRUMENT_TYPE: EI-B
AC$MASS_SPECTROMETRY: MS_TYPE MS
AC$MASS_SPECTROMETRY: ION_MODE POSITIVE
AC$MASS_SPECTROMETRY: IONIZATION_ENERGY 70 eV

MS$FOCUSED_ION: ION_TYPE [M]+*

PK$SPLASH: splash10-0pxr-6490000000-98a9035e85eeea7c02e5
PK$NUM_PEAK: 182
PK$PEAK: m/z int. rel.int.
  30 1.4 14
  31 18.5 185
  36 4 40
  38 2.1 21
  39 10.4 104
  40 2 20
  41 8.8 88
  42 0.68 7
  43 15.6 156
  44 2.2 22
  45 12.7 127
  49 0.22 2
  50 14.8 148
  51 46.5 465
  52 7.6 76
  55 0.25 3
  56 1.5 15
  57 3 30
  59 8.4 84
  61 0.3 3
  62 5.6 56
  63 12.7 127
  64 3.4 34
  65 0.4 4
  66 2.2 22
  69 1.4 14
  69.5 1.6 16
  70 0.19 2
  71 2.7 27
  72 2.4 24
  73 2.7 27
  74 1.03 10
  74.5 1.3 13
  75 31.2 312
  75.5 7.1 71
  76 1.99 20
  76.5 1.7 17
  77 99.99 999
  78 12.9 129
  79 0.33 3
  81 1.5 15
  81.5 1.5 15
  82.5 1.6 16
  83 0.17 2
  83.5 6.5 65
  84 2.2 22
  86 2.5 25
  87 0.39 4
  88 5.5 55
  88.5 9.4 94
  89 12.3 123
  89.5 0.4 4
  90 5.5 55
  91 2.9 29
  92 2.4 24
  93 0.27 3
  94 1.5 15
  96 1.5 15
  96.5 2.1 21
  97 0.37 4
  97.5 3.4 34
  98 3.4 34
  99 6.9 69
  100 1.21 12
  101 5.3 53
  101.5 2.1 21
  102 16.2 162
  102.5 1.05 11
  103 5.4 54
  104 29 290
  105 6.2 62
  106 0.19 2
  106.5 1.7 17
  107 2 20
  109 1.3 13
  110 0.88 9
  111 7.6 76
  111.5 1.9 19
  112 3.9 39
  113 0.24 2
  114 1.9 19
  114.5 3.2 32
  115 2.1 21
  116 0.15 2
  117 1.8 18
  118 2.2 22
  119.5 2.3 23
  120 0.4 4
  121 1.8 18
  123 1.9 19
  124 3.5 35
  125 0.35 4
  126 6.3 63
  127 5.3 53
  128 2.2 22
  129 0.25 3
  130 1.3 13
  134 2 20
  135 1.3 13
  136 0.6 6
  137 3.7 37
  138 3.9 39
  139 3.3 33
  140 0.24 2
  141 2.4 24
  149 6.5 65
  150 10.5 105
  151 2.02 20
  152 9.1 91
  153 4.3 43
  154 1.7 17
  155 0.14 1
  162 1.3 13
  163 6.6 66
  164 2.9 29
  165 0.32 3
  166 3.4 34
  167 2.4 24
  168 1 10
  174 0.11 1
  175 3.4 34
  176 11.4 114
  177 21 210
  178 11.8 118
  179 9.4 94
  180 2.4 24
  181 4.9 49
  182 0.11 1
  183 1.1 11
  185 1 10
  186 2 20
  187 0.11 1
  192 2 20
  193 2.5 25
  194 6.5 65
  195 0.21 2
  199 1.5 15
  202 3.1 31
  203 8.3 83
  204 0.96 10
  205 62.2 622
  206 11.6 116
  207 3.8 38
  208 0.11 1
  211 1.5 15
  212 1.8 18
  213 4.4 44
  214 0.76 8
  215 2.7 27
  216 3.4 34
  221 1.5 15
  223 0.16 2
  228 1.8 18
  229 16.4 164
  230 4.8 48
  231 0.57 6
  232 1.7 17
  233 53 530
  234 9.7 97
  235 0.14 1
  238 1.8 18
  239 54 540
  240 26.9 269
  241 3.72 37
  242 15.6 156
  243 8 80
  244 3.2 32
  255 0.23 2
  256 1.6 16
  257 86 860
  258 16.2 162
  259 2.79 28
  260 5.2 52
  267 47.5 475
  268 67.4 674
  269 2.78 28
  270 24.1 241
  271 4.6 46
  285 4.8 48
  286 1.3 13
  287 4.5 45
  288 4.5 45
//