| Identification | Back Directory | [Name]
FMOC-L-4-TERT-BUTYL-PHE | [CAS]
213383-02-9 | [Synonyms]
FMOC-P-TBU-PHE-OH
FMOC-PHE(P-TBU)-OH
FMOC-PHE(4-TBU)-OH
FMOC-P-TBU-L-PHE-OH
RARECHEM BK PT 0189
Fmoc-L-4-tBu-Phe-OH
Fmoc-π-tBu-L-Phe-OH
Fmoc-L-Phe(4-tBu)-OH
FMOC-L-4-TERT-BUTYL-PHE
FMOC-P-TBU-PHENYLALANINE
Fmoc-L-Phe(4-tBu)-OH, >97%
FMoc-L-4-tButylphenylalanine
FMOC-4-T-BUTYL-L-PHENYLALANINE
Fmoc-L-4-tetr-Butylphenylalanine
FMOC-L-4-TERT-BUTYLPHENYLALANINE
Fmoc-4-tert-butyl-L-phenylalanine
Fmoc-4-tert-butyl-L-phenylalanine≥ 98% (HPLC)
4-tert-Butyl-L-phenylalanine, N-FMOC protected
(9H-Fluoren-9-yl)MethOxy]Carbonyl Phe(4-tBu)-OH
(S)-Fmoc-2-amino-3-(4-tert-butyl-phenyl)propionic acid
N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-(4-T-BUTYL)-L-PHENYLALANINE
4-tert-butyl-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-phenylalanine
4-(1,1-Dimethylethyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-phenylalanine
L-Phenylalanine, 4-(1,1-dimethylethyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
(S)-3-(4-TERT-BUTYL-PHENYL)-2-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-PROPIONIC ACID
(2S)-3-(4-tert-butylphenyl)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanoic acid
(S)-2-((((9H-Fluoren-9-yl)Methoxy)carbonyl)aMino)-3-(4-(tert-butyl)phenyl)propanoic acid | [Molecular Formula]
C28H29NO4 | [MDL Number]
MFCD02094466 | [MOL File]
213383-02-9.mol | [Molecular Weight]
443.53 |
| Chemical Properties | Back Directory | [Boiling point ]
637.9±55.0 °C(Predicted) | [density ]
1.198±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,2-8°C | [form ]
Solid | [pka]
3.81±0.10(Predicted) | [color ]
White to off-white | [InChIKey]
OKEORFXNCSRZFL-VWLOTQADSA-N | [SMILES]
C(O)(=O)[C@H](CC1=CC=C(C(C)(C)C)C=C1)NC(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)=O |
| Hazard Information | Back Directory | [Chemical Properties]
Off-white solid | [Uses]
Fmoc-Phe(4-tBu)-OH is an amino acid derivative with an Fmoc protecting group, which can be used to synthesize rOicPaPhe(p-Me)-NH(2) with platelet aggregation activation inhibitory activity[1]. | [References]
[1] Burke, et al. "Synthesis of novel peptide inhibitors of thrombin‐induced platelet activation." Chemical biology & drug design 68.5 (2006): 235-238. DOI:10.1111/j.1747-0285.2006.00442.x |
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