2767-84-2
2767-84-2
Chemical Structure
(+)-(1S)-Camphorquinone
- CAS No.: 2767-84-2
- Formula:C10H14O2
- Molecular Weight:166.22
IUPAC Name: (1S,4R)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione
InChIKey: VNQXSTWCDUXYEZ-QUBYGPBYSA-N
SMILES: CC1(C)[C@](C2=O)(C)CC[C@H]1C2=O
Biological Activity: (+)-(1S)-Camphorquinone is an isomer of Camphorquinone (HY-W086630). (+)-(1S)-Camphorquinone can be used as a biological material or organic compound for life science related research[1][2][3][4].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
(+)-(1S)-Camphorquinone | 99.70% | (+)-(1S)-Camphorquinone is an isomer of Camphorquinone (HY-W086630). (+)-(1S)-Camphorquinone can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
References
-
[1]. Takamitsu Utsukihara, et al. Reduction of (+)- and (−)-camphorquinones by cyanobacteria. October 2004. Journal of Molecular Catalysis B Enzymatic 31(1):19-24.
- [2]. Maryam M, et al. Synthesis, characterization and evaluation of antidengue activity of enantiomeric Schiff bases derived from S-substituted dithiocarbazate. Turk J Chem. 2020;44(5):1395-1409. Published 2020 Oct 26. [Content Brief]
- [3]. Tahir MI, et al. Discrimination of chiral guests by chiral channels: variable temperature studies by SXRD and solid state 13C NMR of the deoxycholic acid complexes of camphorquinone and endo-3-bromocamphor. Chirality. 2008;20(7):863-870. [Content Brief]
- [4]. García-Ruiz C, et al. Quenched phosphorescence as a detection method in capillary electrophoretic chiral separations. Monitoring the stereoselective biodegradation of camphorquinone by yeast. Anal Chem. 2004;76(2):399-403. [Content Brief]
Keywords
