(+)-2Z,4E-5-[(1S)-3-CHLORO-1-HYDROXY-2,6,6-TRIMETHYL-4-OXO-2-CYClOHEXEN-1-YL]-3-METHYL-2,4-PENTADIENOIC-ACID;3'-CHLORO-ABA
Compound with spectra: 1 NMR
![(+)-2Z,4E-5-[(1S)-3-CHLORO-1-HYDROXY-2,6,6-TRIMETHYL-4-OXO-2-CYClOHEXEN-1-YL]-3-METHYL-2,4-PENTADIENOIC-ACID;3'-CHLORO-ABA](/api/compound/EhGKqfE03sH.png?ph=true&h=300&w=458 "(+)-2Z,4E-5-[(1S)-3-CHLORO-1-HYDROXY-2,6,6-TRIMETHYL-4-OXO-2-CYClOHEXEN-1-YL]-3-METHYL-2,4-PENTADIENOIC-ACID;3'-CHLORO-ABA")
| SpectraBase Compound ID | EhGKqfE03sH |
|---|---|
| InChI | InChI=1S/C15H19ClO4/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 | WCZPRTYVBYYCOO-QMQPWKDKSA-N |
| Mol Weight | 298.77 g/mol |
| Molecular Formula | C15H19ClO4 |
| Exact Mass | 298.097187 g/mol |
| Enantiomer InChIKey | WCZPRTYVBYYCOO-OTFFPYDZSA-N |
| Racemate InChIKey | WCZPRTYVBYYCOO-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-fluoranyl-2,6,6-trimethyl-1-oxidanyl-4-oxidanylidene-cyclohex-2-en-1-yl]-3-methyl-penta-2,4-dienoic acid
(+)-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
(+/-)-9'-FLUOROABSCISIC-ACID
(1'R,6'S)-(+)-8'-FLUOROABSCISIC-ACID
(+)-(1'S,4'R)-5-(4'-ACETOXY-1'-HYDROXY-2',6',6'-TRIMETHYLCYCLOHEX-2'-ENYL)-3-METHYLPENTA-2',4'-DIENOIC-ACID-METHYLESTER
(+)-(1'S,4'S)-5-(4'-ACETOXY-1'-HYDROXY-2',6',6'-TRIMETHYLCYCLOHEX-2'-ENYL)-3-METHYLPENTA-2',4'-DIENOIC-ACID-METHYLESTER
3,4-DEHYDROTHEASPIRONE
Deepoxy-salmoxanthin
8,9-DEHYDROTHEASPIRONE;2,6,10,10-TETRAMETHYL-1-OXASPIRO-[4,5]-DECA-2,6-DIEN-8-ONE
MACARANGIOSIDE-D;(6R,7E,9S)-MEGASTIGMAN-4,7-DIEN-3-ONE-9,13-DIOL-9-O-BETA-D-GLUCOPYRANOSIDE
| 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 |