Boc-trans-Pro(4-azido)-OH·DCHA
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
- Mol File:
- 702679-55-8.mol
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Boc-trans-Pro(4-azido)-OH·DCHA Chemical Properties
- Melting point:
- 55-58 °C
- form
- Solid
- color
- White to off-white
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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
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