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ChemicalBook--->CAS DataBase List--->1196703-48-6

1196703-48-6

1196703-48-6 Structure

1196703-48-6 Structure
IdentificationBack Directory
[Name]

FMOC-PHE-THR(PSI-ME,ME PRO)-OH
[CAS]

1196703-48-6
[Synonyms]

Reaxys ID: 19854654
Fmoc-Phe-Thr[Ψ(Me,Me)Pro]-OH
Fmoc-L-Phe-L-Thr[PSI(Me,Me)Pro
FMOC-PHE-THR(PSI-ME,ME PRO)-OH
Fmoc-L-Phe-L-Thr[PSI(Me,Me)Pro]-OH
FMOC-PHE-THR(ΨME,ME PRO)-OH_1196703-48-6
Fmoc-Phe-Thr[Psi(Me,Me)Pro]-OH≥ 99% (HPLC)
(9H-Fluoren-9-yl)MethOxy]Carbonyl Phe-ThrPsi(Me,Me)Pro-OH
(4S,5R)-3-[N-(9-Fluorenylmethyloxycarbonyl)-L-phenylalaninyl]-2,2,5-trimethyloxazolidine-4-carboxylic acid
(4S,5R)-3-((((9H-fluoren-9-yl)methoxy)carbonyl)-L-phenylalanyl)-2,2,5-trimethyloxazolidine-4-carboxylicacid
(4S,5R)-3-[(2S)-2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-1-oxo-3-phenylpropyl]-2,2,5-trimethyl-4-oxazolidinecarboxylic acid
4-Oxazolidinecarboxylic acid, 3-[(2S)-2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-1-oxo-3-phenylpropyl]-2,2,5-trimethyl-, (4S,5R)-
(4S,5R)-3-[(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-phenylpropanoyl]-2,2,5-trimethyl-1,3-oxazolidine-4-carboxylic acid
[Molecular Formula]

C31H32N2O6
[MDL Number]

MFCD03792291
[MOL File]

1196703-48-6.mol
[Molecular Weight]

528.6
Chemical PropertiesBack Directory
[Boiling point ]

764.4±60.0 °C(Predicted)
[density ]

1.258±0.06 g/cm3(Predicted)
[storage temp. ]

Store at +2°C to +8°C.
[form ]

powder
[pka]

3.14±0.60(Predicted)
[InChIKey]

FFOYZGOZWLCJDO-VHEIIQRDSA-N
[SMILES]

O1[C@H](C)[C@@H](C(O)=O)N(C(=O)[C@@H](NC(OCC2C3=C(C=CC=C3)C3=C2C=CC=C3)=O)CC2=CC=CC=C2)C1(C)C
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H335-H302+H312+H332-H315
[Precautionary statements ]

P280-P301+P312-P362+P364
[HS Code ]

2934999093
Hazard InformationBack Directory
[Chemical Properties]

White to off-white powder
[Uses]

Fmoc-Phe-Thr(psime,MePro)-OH is used as a reactant in the synthesis of GUB06-046, a novel secretin/glucagon-like peptide 1 co-agonist.
[reaction suitability]

reaction type: Fmoc solid-phase peptide synthesis
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