| Weight | 284.356 g/mol |
|---|---|
| Formula | C14H24N2O4 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 6 |
Oseltamivir acid (187227-45-8)
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- A Short Enantioselective Pathway for the Synthesis of the Anti-Influenza Neuramidase Inhibitor Oseltamivir from 1,3-Butadiene and Acrylic Acid (Journal of the American Chemical Society, 2006)
- New, efficient synthesis of oseltamivir phosphate (Tamiflu) via enzymatic desymmetrization of a meso-1,3-cyclohexanedicarboxylic acid diester. (Journal of Organic Chemistry, 2008)
- A short and practical synthesis of oseltamivir phosphate (Tamiflu) from (-)-shikimic acid. (Journal of Organic Chemistry, 2009)
- Amino Acid Changes in Hemagglutinin Contribute to the Replication of Oseltamivir-Resistant H1N1 Influenza Viruses (Journal of Virology, 2012)
- Efficient Access to Oseltamivir Phosphate (Tamiflu) via the OTrimesylate of Shikimic Acid Ethyl Ester (Angewandte Chemie, 2009)
- A novel asymmetric synthesis of oseltamivir phosphate (Tamiflu) from ()-shikimic acid (Tetrahedron-asymmetry, 2009)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCC(CC)OC1C=C(CC(C1NC(=O)C)N)C(=O)O
-
InChIKeyNENPYTRHICXVCS-UHFFFAOYSA-N
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acetamide
+
Reactant
(Alkylation of primary amines)
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