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200616-39-3

200616-39-3 Structure

200616-39-3 Structure
IdentificationBack Directory
[Name]

FMOC-GLU(O-2-PHIPR)-OH
[CAS]

200616-39-3
[Synonyms]

FMoc-Glu(OPp)-OH
Fmoc-L-Glu(PP)-OH
Fmoc-L-Glu(OPP)-OH
FMOC-GLU(O-2-PHIPR)-OH USP/EP/BP
Fmoc-L-Glu(2-phenylisopropyloxy)-OH
(9H-Fluoren-9-yl)MethOxy]Carbonyl Glu(OPis)-OH
Fmoc-L-glutamic acid-γ-2-phenylisopropyl ester
Fmoc-L-glutamic acid 5-(2-phenylisopropyl) ester
Fmoc-L-glutamic acid gamma 2-phenylisopropyl ester
N-Fmoc-L-glutamic acid 5-(2-phenyl-2-propyl) ester
Fmoc-L-glutamic acid g -2-phenylisopropyl ester≥ 98% (HPLC)
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-glutamic acid 5-(1-methyl-1-phenylethyl) ester
L-Glutamic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 5-(1-methyl-1-phenylethyl) ester
(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-5-oxo-5-(2-phenylpropan-2-yloxy)pentanoicaci
(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-5-oxo-5-(2-phenylpropan-2-yloxy)pentanoic acid
(S)-2-(((9H-fluoren-9-yl)methyl9H-fluoren-9-yl)methoxy)carbonylamino)-5-oxo-5-(2-phenylpropan-2-yloxy)pentanoic acid
[Molecular Formula]

C29H29NO6
[MDL Number]

MFCD00672323
[MOL File]

200616-39-3.mol
[Molecular Weight]

487.54
Chemical PropertiesBack Directory
[Boiling point ]

699.0±55.0 °C(Predicted)
[density ]

1.249
[storage temp. ]

Sealed in dry,Store in freezer, under -20°C
[form ]

powder
[pka]

3.69±0.10(Predicted)
[Major Application]

peptide synthesis
[InChIKey]

NPNRKQDJIWMHNG-VWLOTQADSA-N
[SMILES]

N([C@@H](CCC(=O)OC(C)(C)c4ccccc4)C(=O)O)C(=O)OCC1c2c(cccc2)c3c1cccc3
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[WGK Germany ]

WGK 2
[HS Code ]

2924297099
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Chemical Properties]

FMOC-GLU(O-2-PHIPR)-OH is white to pale yellow powder
[Uses]

The 2-PhiPr group can be removed selectively in the presence of tBu-based protecting groups by treatment with 1% TFA in DCM , making this derivative an extremely useful tool for the preparation of cyclic peptides by Fmoc SPPS.
[reaction suitability]

reaction type: Fmoc solid-phase peptide synthesis
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