| Identification | More | [Name]
Fmoc-N'-methyltrityl-L-lysine | [CAS]
167393-62-6 | [Synonyms]
FMOC-L-LYS(MMT)-OH
FMOC-L-LYS(MTT)-OH
FMOC-LYS(4-METHOXYTRITYL)-OH
FMOC-LYS(CH3TRT)-OH
FMOC-LYSINE(4-METHOXYTRITYL)-OH
FMOC-LYSINE(MTT)-OH
FMOC-LYS(MEOTRT)-OH
FMOC-LYS(MMT)-OH
FMOC-LYS(MTT)-OH
FMOC-N-EPSILON-4-METHOXY TRITYL-L-LYSINE
FMOC-N-EPSILON-4-METHOXYYLTRITYL-L-LYSINE
FMOC-N-EPSILON-METHYLTRITYL-L-LYSINE
N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-N-EPSILON-4-METHOXYTRITYL-L-LYSINE
N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-N-EPSILON-P-METHYLTRITYL-L-LYSINE
N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-EPSILON-4-METHOXYTRITYL-L-LYSINE
N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-EPSILON-4-METHYLTRITYL-L-LYSINE
N-ALPHA-FMOC-N-EPSILON-4-METHOXYTRITYL-L-LYSINE
N-ALPHA-FMOC-N-EPSILON-4-METHYLTRITYL-L-LYSINE
N-α-Fmoc-N-δ-methyltrityl-L-lysine
NALPHA-9-Fluorenylmethoxycarbonyl-NOMEGA-(4-methyltrityl)-L-lysine | [Molecular Formula]
C41H40N2O4 | [MDL Number]
MFCD00237166 | [Molecular Weight]
624.77 | [MOL File]
167393-62-6.mol |
| Chemical Properties | Back Directory | [Melting point ]
140 °C(dec.) | [Boiling point ]
798.8±60.0 °C(Predicted) | [density ]
1?+-.0.06 g/cm3(Predicted) | [storage temp. ]
-20°C | [solubility ]
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | [form ]
Solid | [pka]
3.83±0.21(Predicted) | [color ]
White to Almost white | [InChIKey]
YPTNAIDIXCOZAJ-LHEWISCISA-N | [SMILES]
C(O)(=O)[C@H](CCCCNC(C1=CC=C(C)C=C1)(C1=CC=CC=C1)C1=CC=CC=C1)NC(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)=O | [CAS DataBase Reference]
167393-62-6(CAS DataBase Reference) |
| Hazard Information | Back Directory | [Chemical Properties]
White to off-white powder | [Uses]
Fmoc-Lys(Mtt)-OH, is an amino acid derivative, used in chemical synthesis and peptide chemistry. | [General Description]
The side-chain Mtt group can be selectively removed with 1% TFA in DCM [1, 2, 3] or DCM/HFIP/TFE/TES (6.5:2:1:0.5) [4], making this an excellent derivative for the synthesis of branched peptides, peptides modified at the lysine side-chain [5,6], for the construction of templates and multifunctionalized resins for combinatorial synthesis.
The product number for this product was previously 04-12-1137.
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