MassBank Record: JP002726



 3,4-DIHYDROXYHYDROCINNAM1C AC1D-TRI-TMS; EI-B; MS 
Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk) \n

ACCESSION: JP002726
RECORD_TITLE: 3,4-DIHYDROXYHYDROCINNAM1C AC1D-TRI-TMS; EI-B; MS
DATE: 2016.01.19 (Created 2008.10.21, modified 2011.05.06)
AUTHORS: HAYASHI A, DEPT. OF CHEMISTRY, FAC. OF SCI. AND TECHNOLOGY, KINKI UNIV.
LICENSE: CC BY-NC-SA

CH$NAME: 3,4-DIHYDROXYHYDROCINNAM1C AC1D-TRI-TMS CH$COMPOUND_CLASS: N/A CH$FORMULA: C18H34O4Si3 CH$EXACT_MASS: 398.17649 CH$SMILES: O=C(CCc(c1)cc(O[Si](C)(C)C)c(c1)O[Si](C)(C)C)O[Si](C)(C)C CH$IUPAC: InChI=1S/C18H34O4Si3/c1-23(2,3)20-16-12-10-15(14-17(16)21-24(4,5)6)11-13-18(19)22-25(7,8)9/h10,12,14H,11,13H2,1-9H3
AC$INSTRUMENT: SHIMADZU LKB-9000B AC$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$SPLASH: splash10-00b9-8922000000-74671a9e1b8c8a0a4760 PK$NUM_PEAK: 228 PK$PEAK: m/z int. rel.int. 55 3.2 32 56 0.5 5 57 2 20 58 0.8 8 59 5 50 60 0.5 5 61 1.2 12 63 0.02 0 65 0.6 6 66 0.2 2 67 0.9 9 68 0.04 0 69 1.7 17 70 0.3 3 71 0.9 9 72 0.16 2 73 99.99 999 74 8.6 86 75 21.7 217 76 0.17 2 77 1.6 16 78 0.4 4 79 0.4 4 80 0.01 0 81 1.1 11 82 0.3 3 83 1 10 84 0.07 1 85 0.7 7 87 0.3 3 88 0.3 3 89 0.06 1 90 0.1 1 91 1.4 14 92 0.2 2 93 0.06 1 94 0.2 2 95 1.3 13 97 1.3 13 98 0.04 0 99 0.6 6 101 0.4 4 102 0.2 2 103 0.08 1 104 1 10 105 1.4 14 106 0.3 3 107 0.04 0 108 0.2 2 109 0.8 8 110 0.2 2 111 0.05 1 112 0.2 2 113 0.2 2 115 1 10 116 0.11 1 117 3.6 36 118 0.7 7 119 0.5 5 120 0.03 0 121 0.4 4 122 0.2 2 123 0.5 5 124 0.02 0 125 0.2 2 126 0.5 5 127 0.2 2 128 0.02 0 129 1.5 15 130 0.2 2 131 1.5 15 132 0.15 2 133 2.6 26 134 0.6 6 135 0.6 6 136 0.03 0 137 0.4 4 138 0.2 2 139 0.2 2 141 0.02 0 142 0.1 1 143 0.3 3 145 1.3 13 146 0.03 0 147 4.3 43 148 0.8 8 149 9.2 92 150 0.12 1 151 0.9 9 152 0.2 2 153 0.3 3 155 0.02 0 156 0.1 1 157 0.1 1 158 0.1 1 159 0.04 0 160 0.3 3 161 0.8 8 162 0.8 8 163 0.14 1 164 0.4 4 165 0.7 7 166 0.4 4 167 0.05 1 168 0.1 1 169 0.2 2 171 0.3 3 173 0.02 0 175 0.5 5 176 0.3 3 177 2.2 22 178 0.16 2 179 92.9 929 180 14.1 141 181 4.4 44 182 0.05 1 183 0.2 2 185 0.2 2 186 0.1 1 187 0.02 0 189 0.4 4 190 0.2 2 191 1.2 12 192 4 40 193 5.7 57 194 1.1 11 195 0.7 7 196 0.01 0 197 0.2 2 199 0.1 1 201 0.2 2 202 0.01 0 203 0.5 5 204 0.2 2 205 0.8 8 206 0.03 0 207 0.7 7 208 0.2 2 209 0.5 5 210 0.02 0 211 0.3 3 212 0.1 1 213 0.1 1 215 0.01 0 217 0.3 3 218 0.3 3 219 0.8 8 220 0.03 0 221 0.8 8 222 0.2 2 223 1.2 12 224 0.02 0 225 0.1 1 229 0.1 1 231 0.1 1 233 0.02 0 234 0.1 1 235 0.4 4 236 0.3 3 237 0.07 1 238 0.2 2 239 0.3 3 249 0.3 3 250 0.02 0 251 1.1 11 252 0.3 3 253 0.3 3 254 0.03 0 255 0.2 2 257 0.1 1 262 0.1 1 263 0.02 0 264 0.2 2 265 4.4 44 266 1.4 14 267 4.66 47 268 11.7 117 269 4.3 43 270 0.7 7 271 0.02 0 277 0.1 1 278 0.1 1 279 0.4 4 280 1.68 17 281 5.8 58 282 2 20 283 0.4 4 284 0.01 0 285 0.2 2 293 0.6 6 294 0.3 3 295 0.04 0 296 0.1 1 299 0.3 3 307 0.4 4 308 0.06 1 309 0.5 5 310 0.4 4 311 0.3 3 313 0.09 1 314 0.2 2 315 0.2 2 325 0.2 2 326 0.14 1 327 0.5 5 328 0.2 2 354 0.6 6 355 0.03 0 356 0.1 1 368 0.2 2 369 0.2 2 370 0.02 0 381 0.1 1 382 0.3 3 383 11.2 112 384 0.35 4 385 1.7 17 386 0.3 3 392 0.1 1 393 0.02 0 395 0.1 1 396 0.7 7 397 2.5 25 398 7.35 74 399 24.8 248 400 12.6 126 401 2.3 23 402 0.5 5 //