(+)-2Z,4E-5-[(1S)-1-HYDROXY-3-IODO-2,6,6-TRIMETHYL-4-OXO-2-CYClOHEXEN-1-YL]-3-METHYL-2,4-PENTADIENOIC-ACID;3'-IODO-ABA
Compound with spectra: 1 NMR
![(+)-2Z,4E-5-[(1S)-1-HYDROXY-3-IODO-2,6,6-TRIMETHYL-4-OXO-2-CYClOHEXEN-1-YL]-3-METHYL-2,4-PENTADIENOIC-ACID;3'-IODO-ABA](/api/compound/76Dsw2qJ0kc.png?ph=true&h=300&w=458 "(+)-2Z,4E-5-[(1S)-1-HYDROXY-3-IODO-2,6,6-TRIMETHYL-4-OXO-2-CYClOHEXEN-1-YL]-3-METHYL-2,4-PENTADIENOIC-ACID;3'-IODO-ABA")
| SpectraBase Compound ID | 76Dsw2qJ0kc |
|---|---|
| InChI | InChI=1S/C15H19IO4/c1-9(7-12(18)19)5-6-15(20)10(2)13(16)11(17)8-14(15,3)4/h5-7,20H,8H2,1-4H3,(H,18,19)/b6-5+,9-7-/t15-/m1/s1 |
| InChIKey | MKUQZRHAMYKMKC-QMQPWKDKSA-N |
| Mol Weight | 390.22 g/mol |
| Molecular Formula | C15H19IO4 |
| Exact Mass | 390.032804 g/mol |
| Enantiomer InChIKey | MKUQZRHAMYKMKC-OTFFPYDZSA-N |
| Racemate InChIKey | MKUQZRHAMYKMKC-UQIVLYAPSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | ACETONE-D6 |
(+)-2Z,4E-5-[(1S)-3-BrOMO-1-HYDROXY-2,6,6-TRIMETHYL-4-OXO-2-CYClOHEXEN-1-YL]-3-METHYL-2,4-PENTADIENOIC-ACID;3'-BrOMO-ABA
(2Z,4E)-5-[(1S)-3-fluoranyl-2,6,6-trimethyl-1-oxidanyl-4-oxidanylidene-cyclohex-2-en-1-yl]-3-methyl-penta-2,4-dienoic acid
(1'R,6'S)-(+)-8'-FLUOROABSCISIC-ACID
(+/-)-9'-FLUOROABSCISIC-ACID
(+)-(1'S,4'S)-5-(4'-ACETOXY-1'-HYDROXY-2',6',6'-TRIMETHYLCYCLOHEX-2'-ENYL)-3-METHYLPENTA-2',4'-DIENOIC-ACID-METHYLESTER
(+)-(1'S,4'R)-5-(4'-ACETOXY-1'-HYDROXY-2',6',6'-TRIMETHYLCYCLOHEX-2'-ENYL)-3-METHYLPENTA-2',4'-DIENOIC-ACID-METHYLESTER
3,4-DEHYDROTHEASPIRONE
Deepoxy-salmoxanthin
MOMORDOL;1-HYDROXY-1,2-DIMETHYL-2-[8',10'-DIHYDROXY-4',7'-DIMETHYL-11'-HYDROXYMETHYL-TRIDECA]-3-ETHYL-CYCLOHEX-5-EN-4-ONE
8,9-DEHYDROTHEASPIRONE;2,6,10,10-TETRAMETHYL-1-OXASPIRO-[4,5]-DECA-2,6-DIEN-8-ONE
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis and biological activity of 3′-chloro, -bromo, and -iodoabscisic acids, and biological activity of 3′-fluoro-8′-hydroxyabscisic acid | Phytochemistry | 1999 |