![(1R,3S,5R)-2-(tert-Butoxycarbonyl)-2-azabicyclo[3.1.0]hexane-3-carboxylic Acid](https://resource.bocsci.com/structure/197142-34-0.gif)
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| IUPAC Name: | (1R,3S,5R)-2-[(2-methylpropan-2-yl)oxycarbonyl]-2-azabicyclo[3.1.0]hexane-3-carboxylic acid |
| Description: | 1R,3S,5R)-2-(tert-Butoxycarbonyl)-2-azabicyclo[3.1.0]hexane-3-carboxylic Acid acts as a reagent in the preparation of fused bicycles end-capped with peptide derivatives as HCV inhibitors. Synthesis of (tert-butoxycarbonyl)azabicyclohexanecarboxylic acid via stereoselective cyclopropanation of pyrroline |
| Molecular Weight: | 227.26 |
| Molecular Formula: | C11H17NO4 |
| Canonical SMILES: | CC(C)(C)OC(=O)N1C2CC2CC1C(=O)O |
| InChI: | InChI=1S/C11H17NO4/c1-11(2,3)16-10(15)12-7-4-6(7)5-8(12)9(13)14/h6-8H,4-5H2,1-3H3,(H,13,14)/t6-,7-,8+/m1/s1 |
| InChI Key: | VXIIZQXOIDYWBS-PRJMDXOYSA-N |
| Melting Point: | 146 - 149°C |
| Solubility: | Acetone (Slightly, Sonicated), DMSO (Slightly, Sonicated), Methanol (Slightly, H |
| Appearance: | White to Pale Yellow Solid |
| Storage: | -20°C, Hygroscopic |
| References: | Wang, G., et al. Tetrahedron Lett., 54, 6722 (2013); Belema, M., et al. From U.S. Pat. Appl. Publ. (2012), US 20120195857 A1 20120802. |
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