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| | FMOC-GLU(O-2-PHIPR)-OH Basic information |
| Product Name: | FMOC-GLU(O-2-PHIPR)-OH | | Synonyms: | Fmoc-L-Glu(2-phenylisopropyloxy)-OH;N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-glutamic acid 5-(1-methyl-1-phenylethyl) ester;(S)-2-(((9H-fluoren-9-yl)methyl9H-fluoren-9-yl)methoxy)carbonylamino)-5-oxo-5-(2-phenylpropan-2-yloxy)pentanoic acid;Fmoc-L-glutamic acid gamma 2-phenylisopropyl ester;FMoc-Glu(OPp)-OH;Fmoc-L-Glu(PP)-OH;Fmoc-L-glutamic acid-γ-2-phenylisopropyl ester;Fmoc-L-glutamic acid 5-(2-phenylisopropyl) ester | | CAS: | 200616-39-3 | | MF: | C29H29NO6 | | MW: | 487.54 | | EINECS: | | | Product Categories: | | | Mol File: | 200616-39-3.mol |  |
| | FMOC-GLU(O-2-PHIPR)-OH Chemical Properties |
| Boiling point | 699.0±55.0 °C(Predicted) | | density | 1.249 | | storage temp. | Sealed in dry,Store in freezer, under -20°C | | pka | 3.69±0.10(Predicted) | | form | powder |
| | FMOC-GLU(O-2-PHIPR)-OH Usage And Synthesis |
| Chemical Properties | FMOC-GLU(O-2-PHIPR)-OH is white to pale yellow powder | | Uses | The 2-PhiPr group can be removed selectively in the presence of tBu-based protecting groups by treatment with 1% TFA in DCM , making this derivative an extremely useful tool for the preparation of cyclic peptides by Fmoc SPPS. | | reaction suitability | reaction type: Fmoc solid-phase peptide synthesis |
| | FMOC-GLU(O-2-PHIPR)-OH Preparation Products And Raw materials |
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