Search
元素の検索
構造の検索
Thermo Scientific Chemicals
4-(Dimethylamino)piperidine, 97%
CAS: 50533-97-6 | C7H16N2 | 128.22 g/mol
化学物質識別子
CAS50533-97-6
仕様
スペックシート
スペックシートAppearance (Color)Clear colorless to pale yellow
FormLiquid
Identification (FTIR)Conforms
Refractive Index1.4735-1.4785 @ 20?C
Assay (GC)≥96.0%
4-(Dimethylamino)piperidine is having molecular features associated with polyamine modulation of N-methyl-D-aspartate receptors. It is utilized as a mechanism for reducing the effects of alcohol dependence.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
4-(Dimethylamino)piperidine is having molecular features associated with polyamine modulation of N-methyl-D-aspartate receptors. It is utilized as a mechanism for reducing the effects of alcohol dependence.
Notes
Incompatible with air, water, oxidizing agents and heat.
4-(Dimethylamino)piperidine is having molecular features associated with polyamine modulation of N-methyl-D-aspartate receptors. It is utilized as a mechanism for reducing the effects of alcohol dependence.
Notes
Incompatible with air, water, oxidizing agents and heat.
RUO – Research Use Only
General References:
- Elliott, R. J. R.; Jarvis, A.; Rajasekaran, M. B.; Menon, M.; Bowers, L.; Boffey, R.; Bayford, M.; Firth-Clark, S.; Key, R.; Aqil, R.; Kirton, S. B.; Niculescu-Duvaz, D.; Fish, L.; Lopes, F.; McLeary, R.; Trindade, I.; Vendrell, E.; Munkonge, F.; Porter, R.; Perrior, T.; Springer, C.; Oliver, A. W.; Pearl, L. H.; Ashworth, A.; Lord, C. J. Design and discovery of 3-aryl-5-substituted-isoquinolin-1-ones as potent tankyrase inhibitors. Med. Chem. Commun. 2015, 6 (9), 1687-1692.
- Matuszewski, M.; Kiliszek, A.; Rypniewski, W.; Lesnikowski, Z. J.; Olejniczak, A. B. Nucleoside bearing boron clusters and their phosphoramidites - building blocks for modified oligonucleotide synthesis. New J. Chem. 2015, 39 (2), 1202-1221.