| Identification | Back Directory | [Name]
N-[menthyloxycarbonyl]-L-leucine | [CAS]
1047650-51-0 | [Synonyms]
(+)-MEN-LEU-OH
(+)-menthyl(O2C)-Leu-OH
N-[menthyloxycarbonyl]-L-leucine
L-Leucine, N-[[[(1S,2R,5S)-5-methyl-2-(1-methylethyl)cyclohexyl]oxy]carbonyl]- | [Molecular Formula]
C17H31NO4 | [MDL Number]
MFCD30480497 | [MOL File]
1047650-51-0.mol | [Molecular Weight]
313.43 |
| Chemical Properties | Back Directory | [Boiling point ]
443.8±24.0 °C(Predicted) | [density ]
1.04±0.1 g/cm3(Predicted) | [form ]
powder | [pka]
3.99±0.21(Predicted) | [Major Application]
peptide synthesis | [InChI]
1S/C17H31NO4/c1-10(2)8-14(16(19)20)18-17(21)22-15-9-12(5)6-7-13(15)11(3)4/h10-15H,6-9H2,1-5H3,(H,18,21)(H,19,20)/t12-,13+,14-,15-/m0/s1 | [InChIKey]
JDNKQMWGCKCHBF-XGUBFFRZSA-N | [SMILES]
O=C(O)[C@H](CC(C)C)NC(O[C@@H]1[C@@H](C(C)C)CC[C@H](C)C1)=O |
| Hazard Information | Back Directory | [Uses]
Menthol-derived mono-protected L-amino acid (MPAA) ligand is for β-arylation C-H functionalization, developed by the Jin Quan Yu group. | [reaction suitability]
reaction type: C-H Activation
reagent type: ligand
reaction type: Peptide Synthesis |
|
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Sigma-Aldrich
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Energy Chemical
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http://www.energy-chemical.com |
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Merck KGaA
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www.sigmaaldrich.cn |
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