Umbelliferone TMS
Compound with spectra: 3 MS (GC)
| SpectraBase Compound ID | 1fTVL2q1ANi |
|---|---|
| InChI | InChI=1S/C12H14O3Si/c1-16(2,3)15-10-6-4-9-5-7-12(13)14-11(9)8-10/h4-8H,1-3H3 |
| InChIKey | QHOSPKLEKYPTTO-UHFFFAOYSA-N |
| Mol Weight | 234.33 g/mol |
| Molecular Formula | C12H14O3Si |
| Exact Mass | 234.071221 g/mol |
| Copyright | Copyright © 2023-2024 Wiley-VCH GmbH. All Rights Reserved. |
|---|---|
| Source of Spectrum | H.H.Maurer, M.Meyer, K.Pfleger, A.A. Weber / University of Saarland, D-66424 Homburg Germany |
| Technique | GC/MS |
| Copyright | Database Compilation Copyright © 2023-2024 John Wiley and Sons, Inc. Copyright © 2023-2024 John Wiley and Sons, Inc., Portions Copyright Wiley-VCH GmbH, Adams Library under license from Diablo Analytical. All Rights Reserved. |
|---|---|
| Source of Spectrum | Biologically and Environmentally Important Organic Compounds: GCMS Library |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | JH-1982-144-0 |
- Umbelliferone, mono-TMS
- 7-trimethylsilyloxy-1-benzopyran-2-one
- Coumarin-M (HO-) TMS
7-(3-METHYLBUT-2-ENOXY)-UMBELLIFERONE
7,7'-(heptamethylenedioxy)dicoumarin
7-Heptoxy-1-benzopyran-2-one
2-Butenal, 2-methyl-4-[(2-oxo-2H-1-benzopyran-7-yl)oxy]-
7-((E-3-formyl-2-butenyl)oxy)-2h-1-benzopyran-2-one
6-DEOXYHAPLOPINOL;7-[(E)-3'-METHYL-4'-HYDROXY-2'-BUTENYLOXY]-COUMARIN
7-[[(2E,4E)-6-OXOHEPTA-2,4-DIENYL]-OXY]-2H-1-BENZOFURAN-2-ONE
[(2-oxo-2H-chromen-7-yl)oxy]acetyl chloride
(R/S)-7-(2-Methyl-4-oxoprop-1-yloxy)-2H-benzopyran-2-one
Methyl 2'-acetoxy-4'-allyloxycinnamate
This compound is available in the following databases:
Maurer, Meyer, Pfleger, Weber: GC-MS Library of Drugs, Poisons, and Their Metabolites 6th Edition
Author: Hans H. Maurer, Markus Meyer, Karl Pfleger, Armin A. Weber
Identification of trace drugs, poisons, and pollutants requires broad coverage of specific compound classes: metabolites, acetylated, methylated, trimethylsilylated, trifluoroacetylated, pentafluoropropionylated, and heptafluorobutyrylated compounds. Learn more.