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ChemicalBook--->CAS DataBase List--->115520-21-3

115520-21-3

115520-21-3 Structure

115520-21-3 Structure
IdentificationBack Directory
[Name]

FMOC-CYS(TRT)-OPFP
[CAS]

115520-21-3
[Synonyms]

FMOC-CYS(TRT)-OPFP
FMOC-L-CYS(TRT)-OPFP
FMOC-CYS(TRT)-OPFP,98%
FMOC-CYSTEINE(TRT)-OPFP
FMOC-CYS(TRT)-OPFP USP/EP/BP
(9H-Fluoren-9-yl)MethOxy]Carbonyl Cys(Trt)-Opfp
FMOC-S-TRITYL-L-CYSTEINE PENTAFLUOROPHENYL ESTER
nα-fmoc-s-trityl-l-cysteine pentafluorophenyl ester
N-ALPHA-FMOC-S-TRITYL-L-CYSTEINE PENTAFLUOROPHENYL ESTER
N^a-FMoc-S-trityl-L-cysteine pentafluorophenyl ester, 98%
Nα-Fmoc-S-trityl-L-cysteine pentafluorophenyl ester
NALPHA-9-Fluorenylmethoxycarbonyl-S-trityl-L-cysteine pentafluorophenyl est
N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-S-TRITYL-L-CYSTEINE PENTAFLUORPHENYL ESTER
(R)-Perfluorophenyl 2-((((9H-fluoren-9-yl)Methoxy)carbonyl)aMino)-3-(tritylthio)propanoate
L-Cysteine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-S-(triphenylmethyl)-, 2,3,4,5,6-pentafluorophenyl ester
2,3,4,5,6-pentafluorophenyl (2R)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-[(triphenylmethyl)sulfanyl]propanoate
(R)-tert-butyl 1-hydroxy-3-(4-methylbenzylthio)propan-2-ylcarbamate(R)-perfluorophenyl 2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(tritylthio)propanoate
[Molecular Formula]

C43H30F5NO4S
[MDL Number]

MFCD00065639
[MOL File]

115520-21-3.mol
[Molecular Weight]

751.76
Chemical PropertiesBack Directory
[Melting point ]

71-73 °C
[Boiling point ]

803.5±65.0 °C(Predicted)
[density ]

1.359±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
[form ]

Solid
[pka]

10.09±0.46(Predicted)
[BRN ]

4225739
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315
[Precautionary statements ]

P302+P352
[Safety Statements ]

22-24/25
[WGK Germany ]

3
[HS Code ]

2930 90 16
Hazard InformationBack Directory
[Uses]

Fmoc-cys(pmeobzl)-oh is used as a reactant in peptide synthesis.
[reaction suitability]

reaction type: Fmoc solid-phase peptide synthesis
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