PEOSCKIZDYJJSE-RCIMUZKGSA-N
Compound with spectra: 2 NMR
| SpectraBase Compound ID | FS8P6FRk2bm |
|---|---|
| InChI | InChI=1S/C23H32O3/c1-17(2)7-5-8-18(3)9-6-10-19(4)13-14-23-15-20(11-12-21(23)24)26-22(25)16-23/h7,9,11-13,20H,5-6,8,10,14-16H2,1-4H3/b18-9+,19-13+/t20-,23+/m1/s1 |
| InChIKey | PEOSCKIZDYJJSE-RCIMUZKGSA-N |
| Mol Weight | 356.5 g/mol |
| Molecular Formula | C23H32O3 |
| Exact Mass | 356.235145 g/mol |
| Enantiomer InChIKey | PEOSCKIZDYJJSE-PFVASDLQSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- REL-(1'R,5'R)-2-(1'-FARNESYL-5'-HYDROXY-2'-OXOCYClOHEX-3'-EN-1'-YL)-ACETIC-ACID-DELTA-LACTONE
2-[(3R,4R)-3-acetoxy-6-keto-4-[(2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenyl]cyclohexen-1-yl]acetic acid
acetic acid [(1R,4E,8E,10R,12E,14S)-16-keto-4,8,12-trimethyl-17-methylene-15-oxabicyclo[12.3.0]heptadeca-4,8,12-trien-10-yl] ester
CRASSUMOLIDE_D
METHYL-15-HYDROXY-GERMACRA-1(10)E,4E,11(13)-TRIEN-6alpha,12-OLIDE-14-OICACID
METHYL-15-HYDROXY-GERMACRA-1(10)E,4Z,11(13)-TRIEN-6alpha,12-OLIDE-14-OICACID
METHYL_15-HYDROXY-GERMACRA-1-(10)-E,4-E,11-(13)-TRIEN-6-ALPHA,12-OLIDE-14-OIC_ACID
GSLRFQSAMMVDEI-YDHNIYMWSA-N
BALCHANOLIDE
HAAGEANOLIDE
TARAXINIC-ACID,METHYLESTER
| Title | Journal or Book | Year |
|---|---|---|
| Structure Confirmation of a Bioactive Lactone Isolated from Otoba parvifolia through the Synthesis of a Model Compound | Journal of Natural Products | 2004 |
| Further farnesyl-homogentisic acid derivatives from Otoba parvifolia | Phytochemistry | 1995 |
KnowItAll NMR Spectral Library
Author: Wiley
The KnowItAll NMR Spectral Library offers a comprehensive collection of NMR reference spectra, including NMR, CNMR, and XNMR, and covers a wide range of compounds including organics, polymers, monomers, metabolites, and more. Learn more.