![Ethyl (1S,5R,6S)-5-(pentan-3-yloxy)-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylate structure](/static/structures/d7105f44112a78bef11cb5e3.svg)
Structural Feature
Reactive Feature
Synthesis Role
Application Context
5-(戊烷-3-基氧基)-7-氧代-双环[4.1.0]庚-3-烯-3-羧酸乙酯 / 奥司他韦中间体 / 奥司他韦环氧物 / Oseltamivir intermediate / Oseltamivir epoxide / Ethyl (3R,4S,5S)-4,5-epoxy-3-(1-ethylpropoxy)cyclohex-1-ene-1-carboxylate / EEC epoxide / MFCD08063944
| CAS Number | 204254-96-6 |
|---|---|
| Product Code | SL1112044 |
| Molecular Formula | C14H22O4 |
| Molecular Weight | 254.32 |
| Appearance | White to off-white solid |
| Melting Point | 56-57 °C |
| Boiling Point | 336.5±42.0 °C (predicted) |
| Density | 1.08±0.1 g/cm3 (predicted) |
| Solubility | Slightly soluble in chloroform and methanol |
| Optical Rotation | Consistent with structure |
| SMILES | CCC(CC)O[C@@H]1C=C(C[C@H]2[C@@H]1O2)C(=O)OCC |
| InChIKey | XZXCGRFGEVXWIT-FRRDWIJNSA-N |
| Description | A chiral epoxy ethyl carboxylate intermediate associated with oseltamivir synthesis, featuring a 7-oxabicyclo[4.1.0]heptene scaffold, epoxide motif, and ethyl ester functionality. |
| Applications | Primarily used as a pharmaceutical intermediate for oseltamivir/oseltamivir phosphate related synthesis, research, and process development. |
![2,4-Dichloro-7H-pyrrolo[2,3-d]pyriMidine structure](/static/structures/63fd87c606a252dbb3ef18c3.svg)
