(S)-(+)-1,2,3,4-Tetrahydro-1-naphthol (CAS 53732-47-1)
See product citations (1)
QUICK LINKS
(S)-(+)-1,2,3,4-Tetrahydro-1-naphthol is a chiral compound that is significant in the field of organic synthesis. It is often utilized as a building block for the synthesis of various optically active molecules and as a chiral auxiliary or resolving agent in asymmetric synthesis. The compound′s utility in constructing complex chemical structures with multiple chiral centers is of particular interest in synthetic chemistry research. Studies involving (S)-(+)-1,2,3,4-Tetrahydro-1-naphthol also focus on its capacity to induce chirality in other molecules through asymmetric induction, thereby enabling the production of enantiomerically pure compounds. Additionally, its application in the synthesis of natural products and biologically active molecules allows researchers to further explore the relationship between molecular structure and biological function.
(S)-(+)-1,2,3,4-Tetrahydro-1-naphthol (CAS 53732-47-1) References
- High-affinity, non-peptide agonists for the ORL1 (orphanin FQ/nociceptin) receptor. | Röver, S., et al. 2000. J Med Chem. 43: 1329-38. PMID: 10753470
- Influence of phenylalanines 77 and 138 on the stereospecificity of aryl sulfotransferase IV. | Sheng, JJ., et al. 2004. Drug Metab Dispos. 32: 559-65. PMID: 15100179
- Benzylic alcohols as stereospecific substrates and inhibitors for aryl sulfotransferase. | Rao, SI. and Duffel, MW. 1991. Chirality. 3: 104-11. PMID: 1863522
- Roles of rat and human aldo-keto reductases in metabolism of farnesol and geranylgeraniol. | Endo, S., et al. 2011. Chem Biol Interact. 191: 261-8. PMID: 21187079
- Probing the inhibitor selectivity pocket of human 20α-hydroxysteroid dehydrogenase (AKR1C1) with X-ray crystallography and site-directed mutagenesis. | El-Kabbani, O., et al. 2011. Bioorg Med Chem Lett. 21: 2564-7. PMID: 21414777
- N-Benzoyl anthranilic acid derivatives as selective inhibitors of aldo-keto reductase AKR1C3. | Sinreih, M., et al. 2012. Bioorg Med Chem Lett. 22: 5948-51. PMID: 22897946
- Structure-activity relationship of flavonoids as potent inhibitors of carbonyl reductase 1 (CBR1). | Arai, Y., et al. 2015. Fitoterapia. 101: 51-6. PMID: 25549925
- Screening baccharin analogs as selective inhibitors against type 5 17β-hydroxysteroid dehydrogenase (AKR1C3). | Zang, T., et al. 2015. Chem Biol Interact. 234: 339-48. PMID: 25555457
- Improvement of operational stability of Ogataea minuta carbonyl reductase for chiral alcohol production. | Honda, K., et al. 2017. J Biosci Bioeng. 123: 673-678. PMID: 28214241
- Chiral stationary phase optimized selectivity liquid chromatography: A strategy for the separation of chiral isomers. | Hegade, RS., et al. 2017. J Chromatogr A. 1515: 109-117. PMID: 28811101
- Chiral stationary phase optimized selectivity supercritical fluid chromatography: A strategy for the separation of mixtures of chiral isomers. | Hegade, RS. and Lynen, F. 2019. J Chromatogr A. 1586: 116-127. PMID: 30583878
- Liquiritin, as a Natural Inhibitor of AKR1C1, Could Interfere With the Progesterone Metabolism. | Zeng, C., et al. 2019. Front Physiol. 10: 833. PMID: 31333491
- Tetralin as a substrate for camphor (cytochrome P450) 5-monooxygenase. | Grayson, DA., et al. 1996. Arch Biochem Biophys. 332: 239-47. PMID: 8806731
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
(S)-(+)-1,2,3,4-Tetrahydro-1-naphthol, 100 mg | sc-253491 | 100 mg | $163.00 |