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ChemicalBook--->CAS DataBase List--->202920-22-7

202920-22-7

202920-22-7 Structure

202920-22-7 Structure
IdentificationBack Directory
[Name]

FMOC-HIS(1-ME)-OH
[CAS]

202920-22-7
[Synonyms]

FMOC-HIS(T-ME)-OH
FMOC-HIS(1-ME)-OH
Fmoc-His(tau-Me)-OH
Fmoc-L-His(1-Me)-OH
FMOC-HISTIDINE(1-ME)-OH
FMoc-1-Methyl-L-histidine
FMOC-N-IM-METHYL-L-HISTIDINE
Nα-Fmoc-Nim-methyl-L-histidine
Nalpha-Fmoc-Nim-methyl-L-histidine
Fmoc-His(1-Me)-OH Fmoc-His(τ- Me)-OH
N-ALPHA-FMOC-N-TAU-METHYL-L-HISTIDINE
Fmoc-1-methyl-L-histidine Novabiochem
Nα-Fmoc-Nim-methyl-L-histidine≥ 99% (HPLC)
(9H-Fluoren-9-yl)MethOxy]Carbonyl His(1-Me)-OH
N-(9-FLUORENYLMETHOXYCARBONYL)-N-TAU-METHYL-L-HISTIDINE
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-1-methyl-L-histidine
L-Histidine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-1-methyl-
Na-(((9H-Fluoren-9-yl)methoxy)carbonyl)-Nt-methyl-L-histidine
N-(9-FLUORENYLMETHOXYCARBONYL)-N-IMIDAZOLE-1-METHYL-L-HISTIDINE
(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(1-methylimidazol-4-yl)propanoic acid
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(1-methyl-1H-imidazol-4-yl)propanoic acid
(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-(1-methyl-1H-imidazol-4-yl)propanoic acid
[Molecular Formula]

C22H21N3O4
[MDL Number]

MFCD02259495
[MOL File]

202920-22-7.mol
[Molecular Weight]

391.42
Chemical PropertiesBack Directory
[Boiling point ]

686.7±55.0 °C(Predicted)
[density ]

1.34±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

DMF: 10 mg/ml; DMSO: 10 mg/ml; PBS (pH 7.2): 0.2 mg/ml
[form ]

A solid
[pka]

3.06±0.10(Predicted)
[color ]

White to yellow
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501
[WGK Germany ]

WGK 3 highly water endangering
[HS Code ]

2933 29 90
Hazard InformationBack Directory
[Chemical Properties]

White to off-white powder
[Uses]

Fmoc-his(1-me)-oh is an intermediate used in the synthesis of methylhistidine and histidine methylated analogs of OVA sequence.
[reaction suitability]

reaction type: Fmoc solid-phase peptide synthesis
[storage]

Store at -20°C
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