| Identification | More | [Name]
FMOC-L-3-Fluorophe | [CAS]
198560-68-8 | [Synonyms]
fluorenylmethoxycarbonyl-l-3-fluorophenylalanine
FMOC-3-FLUORO-L-PHE
FMOC-3-FLUORO-L-PHENYLALANINE
FMOC-L-3-FLUOROPHE
FMOC-L-3-FLUOROPHENYLALANINE
FMOC-L-PHE(3-F)-OH
FMOC-M-FLUORO-L-PHENYLALANINE
FMOC-M-FLUORO-PHENYLALANINE
FMOC-M-FLUORO-PHE-OH
FMOC-PHE(3-F)-OH
FMOC-PHE(M-F)-OH
FMOC-(S)-2-AMINO-3-(3'-FLUOROPHENYL)PROPANOIC ACID
L-3-FLUOROPHENYLALANINE, FMOC PROTECTED
N-(9-FLUORENYLMETHOXYCARBONYL)-3-FLUOROPHENYL-L-ALANINE
N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-E-FLUORO-L-PHENYLALANINE
N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-L-3-FLUORO-PHENYLALANINE
RARECHEM BK PT 0027
(S)-2-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-3-(3-FLUORO-PHENYL)-PROPIONIC ACID
(S)-N-FMOC-3-FLUOROPHENYLALANINE
(S)-N-FMOC-3-FLUOROPHENYLALANINE 98% | [Molecular Formula]
C24H20FNO4 | [MDL Number]
MFCD00672328 | [Molecular Weight]
405.42 | [MOL File]
198560-68-8.mol |
| Chemical Properties | Back Directory | [Appearance]
white powder or chunks | [Melting point ]
155.8 °C | [alpha ]
-39 º (c=1,DMF) | [Boiling point ]
618.1±55.0 °C(Predicted) | [density ]
1.2642 (estimate) | [storage temp. ]
2-8°C
| [form ]
solid | [pka]
3.70±0.10(Predicted) | [color ]
beige | [Major Application]
peptide synthesis | [InChI]
1S/C24H20FNO4/c25-16-7-5-6-15(12-16)13-22(23(27)28)26-24(29)30-14-21-19-10-3-1-8-17(19)18-9-2-4-11-20(18)21/h1-12,21-22H,13-14H2,(H,26,29)(H,27,28)/t22-/m0/s1 | [InChIKey]
DWSDVARCJDOADL-QFIPXVFZSA-N | [SMILES]
FC1=CC=CC(C[C@H](NC(OCC2C3=C(C4=C2C=CC=C4)C=CC=C3)=O)C(O)=O)=C1 | [CAS DataBase Reference]
198560-68-8(CAS DataBase Reference) |
| Safety Data | Back Directory | [Safety Statements ]
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [Hazard Note ]
Harmful | [HazardClass ]
IRRITANT | [HS Code ]
2922498590 | [Storage Class]
11 - Combustible Solids |
| Hazard Information | Back Directory | [Chemical Properties]
white powder or chunks | [Uses]
Phenylalanine derivative was introduced in collaboration with Yu and coworkers in reflection to a methodology reported in C-H Activation. | [reaction suitability]
reaction type: Fmoc solid-phase peptide synthesis |
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