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| | Boc-trans-Pro(4-azido)-OH·DCHA Basic information |
| Product Name: | Boc-trans-Pro(4-azido)-OH·DCHA | | Synonyms: | (2S,4R)-Boc- 4-azido-pyrrolidine-2-carboxylic acid·DCHA;Boc-trans-Pro(4-azido)-OH·DCHA;Fmoc-(2S,4R)-4-azidoproline;Fmoc-(4R)-azido-L-Proline≥ 99% (HPLC);Fmoc-L-Pro(4R-N3)-OH (2S,4R);Fmoc-(4R)-azido-L-Proline;trans-4-Azido-N-Fmoc-L-proline;(2S,4R)-1-(((9H-fluoren-9-yl)methoxy)carbonyl)-4-azidopyrrolidine-2-carboxylic acid | | CAS: | 702679-55-8 | | MF: | C20H18N4O4 | | MW: | 378.38132 | | EINECS: | | | Product Categories: | | | Mol File: | 702679-55-8.mol |  |
| | Boc-trans-Pro(4-azido)-OH·DCHA Chemical Properties |
| Melting point | 55-58 °C | | form | Solid | | color | White to off-white |
| | Boc-trans-Pro(4-azido)-OH·DCHA Usage And Synthesis |
| Chemical Properties | White crystalline powder | | Uses | (2S,4R)-Fmoc-L-Pro(4-N3)-OH is a click chemistry reagent containing an azide[1]. (2S,4R)-Fmoc-L-Pro(4-N3)-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups. | | References | [1] Lewandowska U, et al. Hierarchical supramolecular assembly of sterically demanding π-systems by conjugation with oligoprolines. Angew Chem Int Ed Engl. 2014 Nov 10;53(46):12537-41. doi: 10.1002/anie.201408279. Epub 2014 Oct 10. DOI:10.1002/anie.201408279 |
| | Boc-trans-Pro(4-azido)-OH·DCHA Preparation Products And Raw materials |
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