| Identification | Back Directory | [Name]
(3R,4R,5S)-ethyl 4,5-diacetamido-3-(pentan-3-yloxy)cyclohex-1- enecarboxylate | [CAS]
1191921-01-3 | [Synonyms]
Oseltamivir-acetate
Oseltamivir Impurity456
Oseltamivir Impurity455
(3R,4R,5S)-ethyl 4,5-diacetamido-3-(pentan-3-yloxy)cyclohex-1- enecarboxylate | [Molecular Formula]
C18H30N2O5 | [MDL Number]
MFCD34167494 | [MOL File]
1191921-01-3.mol | [Molecular Weight]
354.44 |
| Chemical Properties | Back Directory | [Boiling point ]
572.2±50.0 °C(Predicted) | [density ]
1.10±0.1 g/cm3(Predicted) | [storage temp. ]
Store at -20°C | [form ]
Solid | [pka]
14.44±0.70(Predicted) | [color ]
White to off-white |
| Hazard Information | Back Directory | [Uses]
Oseltamivir-acetate is an impurity of Oseltamivir. Oseltamivir is a neuraminidase inhibitor recommended for the treatment and prophylaxis of influenza A and B[1][2]. | [Biological Activity]
Oseltamivir-acetate is an impurity of Oseltamivir. Oseltamivir is a neuraminidase inhibitor recommended for the treatment and prophylaxis of influenza A and B[1][2]. | [storage]
Store at -20°C | [References]
[1]. Huang H, et al. Transplacental transfer of Oseltamivir phosphate and its metabolite Oseltamivir carboxylate using the ex vivo human placenta perfusion model in Chinese Hans population. J Matern Fetal Neonatal Med. 2016 Aug 8:1-5. [2]. de Oliveira JT, et al. Anti-influenza neuraminidase inhibitor Oseltamivir phosphate induces canine mammary cancer cell aggressiveness. PLoS One. 2015 Apr 7;10(4):e0121590. |
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