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| FMOC-MET(O2)-OH Basic information |
| Product Name: | FMOC-MET(O2)-OH | | Synonyms: | FMOC-L-METHIONINE-SULFONE;FMOC-L-MET(O2)-OH;FMOC-METHIONINE(O2)-OH;FMOC-MET(O2)-OH;(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-4-(methylsulfonyl)butanoic acid;FMoc-Met(O)2-OH FMoc-L-Methionine sulfone;N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-L-METHIONINE SULFONE;N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-L-METHIONINESULFON | | CAS: | 163437-14-7 | | MF: | C20H21NO6S | | MW: | 403.45 | | EINECS: | | Product Categories: | | Mol File: | 163437-14-7.mol |
| FMOC-MET(O2)-OH Chemical Properties |
| Boiling point | 709.5±60.0 °C(Predicted) | | density | 1.359 | | storage temp. | Sealed in dry,Room Temperature | | pka | 3.52±0.10(Predicted) | | form | Powder | | color | White | | InChIKey | KJLKPACOHZKRFM-SFHVURJKSA-N | | CAS DataBase Reference | 163437-14-7(CAS DataBase Reference) |
| WGK Germany | WGK 2 water endangering | | HS Code | 2930 90 98 |
| FMOC-MET(O2)-OH Usage And Synthesis |
| Description | FMOC-Met (O2)-OH is the N-alpha protected form of L-methionine mediated by FMOC group (9-Fluorenylmethyloxycarbonyl). It is useful to act as a building block in peptide synthesis. For example, it, as well as its derivative Tbfmoc-Met-OH can be used as a building block for the solid phase synthesis of ubiquitin C-hydrazide. It can also be used for synthesizing some novel cyclic peptides with pharmacological effects such as treatment of inflammatory disease.
| | Chemical Properties | White powder | | References | http://www.sigmaaldrich.com/technical-documents/articles/chemfiles/natural-amino-acid.html
https://www.iris-biotech.de/de/faa1490/Anderson, S. N., et al. "Microarrayed compound screening (microARCS) to identify activators and inhibitors of AMP-activated protein kinase."Journal of Biomolecular Screening 9.2(2004):112-121.
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http://www.google.com/patents/US6511961
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| FMOC-MET(O2)-OH Preparation Products And Raw materials |
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