ACCESSION: MSBNK-Fac_Eng_Univ_Tokyo-JP003069
RECORD_TITLE: (E)-2-1-(4-METHYLPHENYL)-3-(1-PYRROLIDINYL)-1-PROPENYL-PYRIDINE; EI-B; MS
DATE: 2016.01.19 (Created 2008.10.21, modified 2011.05.06)
AUTHORS: SASAKI S, TOYOHASHI UNIV. OF TECH.
LICENSE: CC BY-NC-SA

CH$NAME: (E)-2-1-(4-METHYLPHENYL)-3-(1-PYRROLIDINYL)-1-PROPENYL-PYRIDINE
CH$COMPOUND_CLASS: N/A
CH$FORMULA: C₁₉H₂₂N₂
CH$EXACT_MASS: 278.17830
CH$SMILES: Cc(c3)ccc(c3)C(=C([H])CN(C2)CCC2)c(c1)nccc1
CH$IUPAC: InChI=1S/C19H22N2/c1-16-7-9-17(10-8-16)18(19-6-2-3-12-20-19)11-15-21-13-4-5-14-21/h2-3,6-12H,4-5,13-15H2,1H3/b18-11+
CH$LINK: INCHIKEY CBEQULMOCCWAQT-WOJGMQOQSA-N
CH$LINK: COMPTOX DTXSID3023718

AC$INSTRUMENT: Unknown
AC$INSTRUMENT_TYPE: EI-B
AC$MASS_SPECTROMETRY: MS_TYPE MS
AC$MASS_SPECTROMETRY: ION_MODE POSITIVE

MS$FOCUSED_ION: ION_TYPE [M]+*

PK$SPLASH: splash10-0a4i-2690000000-a4b47440bb135b0a9add
PK$NUM_PEAK: 173
PK$PEAK: m/z int. rel.int.
  38 3.1 31
  39 0.7 7
  40 4.8 48
  41 0.9 9
  42 1.9 19
  43 0.3 3
  50 0.3 3
  51 0.39 4
  52 1.9 19
  53 1.9 19
  54 7.4 74
  55 0.19 2
  56 0.5 5
  57 0.5 5
  61 0.7 7
  62 0.21 2
  63 0.8 8
  64 2.9 29
  65 0.9 9
  66 0.09 1
  67 1.3 13
  68 1.2 12
  69 3.8 38
  70 0.01 0
  73 0.1 1
  74 0.9 9
  75 1 10
  76 0.13 1
  77 2.9 29
  78 6.4 64
  79 2.9 29
  80 0.24 2
  81 0.5 5
  82 1.9 19
  83 6.9 69
  84 1.79 18
  85 1.3 13
  86 0.3 3
  87 0.1 1
  88 0.08 1
  89 3.7 37
  90 1.9 19
  91 2.9 29
  92 0.11 1
  93 6 60
  94 1.5 15
  95 0.3 3
  96 1.49 15
  97 2.7 27
  98 0.1 1
  101 1.1 11
  102 0.33 3
  103 4.2 42
  104 4.2 42
  105 3.3 33
  106 0.02 0
  107 0.1 1
  108 0.1 1
  109 0.8 8
  110 0.19 2
  111 0.9 9
  114 1.1 11
  115 5.3 53
  116 0.37 4
  117 11.9 119
  118 7.4 74
  119 1.9 19
  120 0.01 0
  124 1.3 13
  125 0.1 1
  126 0.9 9
  127 0.26 3
  128 4 40
  129 3.2 32
  130 2.9 29
  131 0.35 4
  132 1.3 13
  133 1.3 13
  134 0.9 9
  138 0.17 2
  139 2.9 29
  140 1.2 12
  141 1.5 15
  142 0.01 0
  143 1 10
  144 2 20
  145 1.8 18
  146 0.01 0
  147 0.8 8
  151 1.5 15
  152 2.9 29
  153 0.17 2
  154 1.7 17
  155 1.1 11
  156 1.7 17
  157 0.22 2
  158 2.2 22
  159 1.7 17
  160 0.7 7
  163 0.01 0
  164 1.2 12
  165 3.3 33
  166 2.5 25
  167 0.64 6
  168 1.9 19
  169 0.4 4
  170 1 10
  171 0.11 1
  172 2.9 29
  173 5.6 56
  174 1.4 14
  176 0.07 1
  177 1.5 15
  178 2.9 29
  179 2.9 29
  180 0.89 9
  181 11.9 119
  182 6.9 69
  183 4.9 49
  184 0.19 2
  185 1.9 19
  186 2.4 24
  187 1.9 19
  188 0.01 0
  189 0.3 3
  190 2.9 29
  191 9.4 94
  192 1.04 10
  193 22.4 224
  194 19.4 194
  195 3.4 34
  196 1.34 13
  197 3.4 34
  198 1.4 14
  199 0.8 8
  200 1.74 17
  201 3.4 34
  202 0.1 1
  203 0.3 3
  204 0.54 5
  205 4.9 49
  206 17.4 174
  207 36.7 367
  208 9.15 92
  209 99.99 999
  210 16.9 169
  211 1.9 19
  217 0.03 0
  218 1.1 11
  219 1.9 19
  220 2.9 29
  221 1.69 17
  222 5.4 54
  223 1.9 19
  224 0.4 4
  232 0.04 0
  233 0.4 4
  234 1.9 19
  235 2.9 29
  236 0.04 0
  246 0.4 4
  247 1.4 14
  248 1.9 19
  249 0.19 2
  262 0.4 4
  263 1.4 14
  275 0.7 7
  276 0.25 3
  277 6.5 65
  278 58.5 585
  279 15.6 156
  280 0.25 3
  281 0.1 1
//