BD9283331
                    (1R,3S,5R)-2-(tert-Butoxycarbonyl)-2-azabicyclo[3.1.0]hexane-3-carboxylic acid , 97% , 197142-34-0
CAS NO.:197142-34-0
Empirical Formula: C11H17NO4
Molecular Weight: 227.26
MDL number: MFCD08691405
EINECS: 815-186-6
| Pack Size | Price | Stock | Quantity | 
| 100mg | RMB199.20 | In Stock | 
                                                 | 
                                        
| 250mg | RMB464.80 | In Stock | 
                                                 | 
                                        
| 1g | RMB1257.60 | In Stock | 
                                                 | 
                                        
| 5g | RMB5126.40 | In Stock | 
                                                 | 
                                        
| others | Enquire | 
Update time: 2022-07-08
                    PRODUCT Properties
| Boiling point: | 355.9±25.0 °C(Predicted) | 
                                    
| Density | 1.276±0.06 g/cm3(Predicted) | 
                                    
| storage temp. | 2-8°C | 
                                    
| solubility | Acetone (Slightly, Sonicated), DMSO (Slightly, Sonicated), Methanol (Slightly, Heated) | 
                                    
| pka | 4.03±0.20(Predicted) | 
                                    
| form | Solid | 
                                    
| color | White to Pale Yellow | 
                                    
| Stability: | Hygroscopic | 
                                    
| 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 | 
                                    
| InChIKey | VXIIZQXOIDYWBS-PRJMDXOYSA-N | 
                                    
| SMILES | [C@]12([H])[C@]([H])(C1)C[C@@H](C(O)=O)N2C(OC(C)(C)C)=O | 
                                    
Description and Uses
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
Safety
| Symbol(GHS) | ![]() GHS07  | 
                                    
| Signal word | Warning | 
| Hazard statements | H315-H319-H335 | 
| Precautionary statements | P261-P305+P351+P338 | 

![(1R,3S,5R)-2-(tert-Butoxycarbonyl)-2-azabicyclo[3.1.0]hexane-3-carboxylic acid](https://img.chemicalbook.com/CAS/GIF/197142-34-0.gif)


![AcetaMide, N-[(1S)-2-[(1S,3S,5S)-3-cyano-2-azabicyclo[3.1.0]hex-2-yl]-1-(3-hydroxytricyclo[3.3.1.13,7]dec-1-yl)-2-oxoethyl]-2,2,2-trifluoro-](https://img.chemicalbook.com/CAS/20210111/GIF/865999-70-8.gif)
![2-Azabicyclo[3.1.0]hexane-3-carbonitrile, 2-[(2R)-2-aMino-2-(3-hydroxytricyclo[3.3.1.13,7]dec-1-yl)acetyl]-, (1S,3R,5S)-](https://img.chemicalbook.com/CAS/20200611/GIF/1564266-03-0.gif)
![(1S,3S,5S)-2-(tert-Butoxycarbonyl)-2-azabicyclo[3.1.0]hexane-3-carboxylicacid](https://img.chemicalbook.com/StructureFile/ChemBookStructure20/GIF/CB2825254.gif)
