![(3R,4R,5R)-4-(1-Ethylpropoxy)-3-hydroxy-5-[(methylsulfonyl)oxy]-1-cyclohexene-1-carboxylic Acid Ethyl Ester](https://resource.bocsci.com/structure/204254-94-4.gif)
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| IUPAC Name: | ethyl (3R,4R,5R)-3-hydroxy-5-methylsulfonyloxy-4-pentan-3-yloxycyclohexene-1-carboxylate |
| Description: | (3R,4R,5R)-4-(1-Ethylpropoxy)-3-hydroxy-5-[(methylsulfonyl)oxy]-1-cyclohexene-1-carboxylic Acid Ethyl Ester is an analog of (1R,5S,6S)-rel-5-(1-Ethylpropoxy)-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylic Acid Methyl Ester (E925665) which is an intermediate in the synthesis of neuraminidase inhibitors. |
| Molecular Weight: | 350.43 |
| Molecular Formula: | C15H26O7S |
| Canonical SMILES: | CCC(CC)OC1C(CC(=CC1O)C(=O)OCC)OS(=O)(=O)C |
| InChI: | InChI=1S/C15H26O7S/c1-5-11(6-2)21-14-12(16)8-10(15(17)20-7-3)9-13(14)22-23(4,18)19/h8,11-14,16H,5-7,9H2,1-4H3/t12-,13-,14-/m1/s1 |
| InChI Key: | CNFGUAGRJCDUDT-MGPQQGTHSA-N |
| Solubility: | Chloroform (Slightly), Dichloromethene (Slightly), Ethyl Acetate, Methanol |
| Appearance: | Colourless Oil to Gel |
| Storage: | 4°C |
| References: | Braese, S. et al. Sci. Synth. 41, 543 (2010); Jarinrat K. et al. Bioorg. Med. Chem. Lett., 20, 2152 (2012). |
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