Name | N'-Fmoc-L-lysine |
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Synonyms |
(2S)-2-Ammonio-6-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}hexanoate
MFCD00038365 H-L-Lys(Fmoc)-OH L-Lysine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]- N6-Fmoc-L-lysine REF DUPL: H-Lys(Fmoc)-OH H-LYS(FMOC)-OH N6-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-lysine LYSINE(FMOC)-OH N'-(9-Fluorenylmethyloxycarbonyl)-L-lysine 1-Pentanaminium, 1-carboxy-5-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, inner salt, (1S)- Fmoc-l-lysine N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-lysine |
Description | H-Lys(Fmoc)-OH is a lysine derivative[1]. |
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Related Catalog | |
In Vitro | Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1]. |
References |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 609.9±55.0 °C at 760 mmHg |
Molecular Formula | C21H24N2O4 |
Molecular Weight | 368.426 |
Flash Point | 322.6±31.5 °C |
Exact Mass | 368.173615 |
PSA | 101.65000 |
LogP | 3.19 |
Vapour Pressure | 0.0±1.8 mmHg at 25°C |
Index of Refraction | 1.601 |
Storage condition | Store at RT. |
Hazard Codes | Xi |
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~94% 84624-28-2 |
Literature: Ovaa, Huib; Van Swieten, Paul F.; Kessler, Benedikt M.; Leeuwenburgh, Michiel A.; Fiebiger, Edda; Van den Nieuwendijk, Adrianus M. C. H.; Galardy, Paul J.; Van der Marel, Gijsbert A.; Ploegh, Hidde L.; Overkleeft, Herman S. Angewandte Chemie - International Edition, 2003 , vol. 42, # 31 p. 3626 - 3629 |
~% 84624-28-2 |
Literature: Tetrahedron, , vol. 61, # 9 p. 2493 - 2503 |
~% 84624-28-2 |
Literature: Angewandte Chemie - International Edition, , vol. 37, # 11 p. 1524 - 1528 |
~% 84624-28-2 |
Literature: Organic Preparations and Procedures International, , vol. 26, # 5 p. 578 - 580 |
~% 84624-28-2 |
Literature: Synthesis, , # 2 p. 119 - 122 |
Precursor 7 | |
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DownStream 0 |