- FMOC-MET(O2)-OH
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- $1.00
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2019-07-06
- CAS:163437-14-7
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 20kg
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| | FMOC-MET(O2)-OH Basic information |
| Product Name: | FMOC-MET(O2)-OH | | Synonyms: | FMOC-L-METHIONINE-SULFONE;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;N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-L-METHIONINESULFONE | | 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 | | solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | | pka | 3.52±0.10(Predicted) | | form | Powder | | color | White | | Major Application | peptide synthesis | | InChI | InChI=1S/C20H21NO6S/c1-28(25,26)11-10-18(19(22)23)21-20(24)27-12-17-15-8-4-2-6-13(15)14-7-3-5-9-16(14)17/h2-9,17-18H,10-12H2,1H3,(H,21,24)(H,22,23)/t18-/m0/s1 | | InChIKey | KJLKPACOHZKRFM-SFHVURJKSA-N | | SMILES | C(O)(=O)[C@@H](NC(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)=O)CCS(C)(=O)=O | | CAS DataBase Reference | 163437-14-7(CAS DataBase Reference) |
| WGK Germany | WGK 2 water endangering | | HS Code | 2930 90 98 | | Storage Class | 11 - Combustible Solids |
| | 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 | | reaction suitability | reaction type: Fmoc solid-phase peptide synthesis | | 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 |
| | FMOC-MET(O2)-OH Preparation Products And Raw materials |
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