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| N-Boc-L-trans-4,5-Methanoproline Basic information | Uses |
Product Name: | N-Boc-L-trans-4,5-Methanoproline | Synonyms: | N-Boc-L-trans-4,5-Methanoproline;(1R,3S,5R)-2-[(tert-Butoxy)carbonyl]-2-azabicyclo[3.1.0]hexane-3-carboxyl+;N-Boc-L-trans-2-azabicyclo[3.1.0]hexane-3-carboxylic acid;2-Azabicyclo[3.1.0]hexane-2,3-dicarboxylic acid, 2-(1,1-dimethylethyl) ester, (1R,3S,5R)-;EOS-61213;(1R,3S,5R)-2-(tert-butoxyCARBONYL)-2-AZABICLO[3.1.0]hexane-3-carboxylic acid;(1R,3S,5R)-2-Boc-2-azabicyclo[3.1.0]hexane-3-carboxylic Acid;N-tert-butoxycarbonyl-l-trans-2-azabicyclo 3.1.0 hexane-3-carboxylic acid | CAS: | 197142-34-0 | MF: | C11H17NO4 | MW: | 227.26 | EINECS: | 815-186-6 | Product Categories: | | Mol File: | 197142-34-0.mol | |
| N-Boc-L-trans-4,5-Methanoproline Chemical 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 |
| N-Boc-L-trans-4,5-Methanoproline Usage And Synthesis |
Uses | N-Boc-L-trans-4,5-Methanoproline belongs to carboxylic acid derivatives and can be used as pharmaceutical intermediates. | 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 |
| N-Boc-L-trans-4,5-Methanoproline Preparation Products And Raw materials |
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