| Identification | Back Directory | [Name]
FMOC-LYS(MCA)-OH | [CAS]
386213-32-7 | [Synonyms]
FMOC-LYS(MCA)-OH
FMOC-LYSINE(MCA)-OH
Fmoc-Lys(Mca)-OH, >97%
N-α-Fmoc-N-ω-7-methoxycoumarin-4-acetyl-L-Lys-OH
N-α-Fmoc-N-ω-7-methoxycoumarin-4-acetyl-L-lysine
(9H-Fluoren-9-yl)MethOxy]Carbonyl L-Lysine(MCA)-OH
N-ALPHA-FMOC-N-EPSILON-7-METHOXYCOUMARIN-4-ACETYL-L-LYSINE
N-α-(9-Fluorenylmethoxycarbonyl)-N-ε-[(7-methoxycoumarin-4-yl)acetyl]-L-lysine
N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-N-EPSILON-(7-METHOXYCOUMARIN-4-YL) ACETYL-L-LYSINE
N2-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N6-(2-(7-methoxy-2-oxo-2H-chromen-4-yl)acetyl)-L-lysine
L-Lysine,N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-N6-[(7-methoxy-2-oxo-2H-1-benzopyran-4-yl)acetyl]-
L-Lysine, N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-N6-[2-(7-methoxy-2-oxo-2H-1-benzopyran-4-yl)acetyl]-
(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-6-[[2-(7-methoxy-2-oxochromen-4-yl)acetyl]amino]hexanoic acid
(S)-2-((((9H-Fluoren-9-yl)Methoxy)carbonyl)aMino)-6-(2-(7-Methoxy-2-oxo-2H-chroMen-4-yl)acetaMido)hexanoic acid
(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-6-[2-(7-methoxy-2-oxo-2H-chromen-4-yl)acetamido]hexanoic acid
(S)-2-(N-(((9H-fluoren-9-yl)methyl9H-fluoren-9-yl)methoxy)carbonyl)acetamido)-6-(7-methoxy-2-oxo-2H-chromen-4-ylamino)hexanoic acid | [Molecular Formula]
C33H32N2O8 | [MDL Number]
MFCD03791024 | [MOL File]
386213-32-7.mol | [Molecular Weight]
584.62 |
| Chemical Properties | Back Directory | [Boiling point ]
885.2±65.0 °C(Predicted) | [density ]
1.309±0.06 g/cm3(Predicted) | [storage temp. ]
-20°C | [form ]
powder | [pka]
3.87±0.21(Predicted) | [Major Application]
peptide synthesis | [InChIKey]
BWJJONDPLYEAMC-NDEPHWFRSA-N | [SMILES]
N([C@@H](CCCCNC(=O)Cc4c5c([o][c](c4)=O)cc(cc5)OC)C(=O)O)C(=O)OCC1c2c(cccc2)c3c1cccc3 |
| Hazard Information | Back Directory | [Uses]
Fmoc-Lys(Mca)-OH can be used as a building block to prepare fluorescent labeled peptides by solid-phase peptide synthesis. It is also used to synthesize luminescent lanthanide(III)-based chelates for spectroscopic applications, in particular, to label folded proteins or DNA. | [reaction suitability]
reaction type: Fmoc solid-phase peptide synthesis |
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