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210820-99-8

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210820-99-8 Structure

210820-99-8 Structure
IdentificationBack Directory
[Name]

FMOC-L-HIS(BOC)-OH DCHA
[CAS]

210820-99-8
[Synonyms]

FMOC-HIS(BOC)-OH DCHA
Fmoc-L-His(Boc)-OH CHA
FMOC-L-HIS(BOC)-OH DCHA
Fmoc-His(Boc)-OHcyclohexyla
Fmoc-His(Boc)-OH-CHA Novabiochem
N(ALPHA)-FMOC-N(IM)-BOC-L-HISTIDINE
fmoc-his(boc)-oh cyclohexylamine salt
Fmoc-His(Boc)-OH cyclohexylammonium salt
(9H-Fluoren-9-yl)MethOxy]Carbonyl His(Boc)-OH·CHA
nα-fmoc-n(im)-boc-l-histidine cyclohexylamine salt
Nα-Fmoc-Nim-Boc-L-histidine cyclohexylammonium salt
N^a-Fmoc-1-Boc-L-histidine cyclohexylammonium salt, 95%
N-alpha-(9-Fluorenylmethyloxycarbonyl)-N-im-(t-butyloxycarbonyl)-L-histidinecyclohexylamine
N-ALPHA-(9-FLUOROENYLMETHYLOXYCARBONYL)-N-IM-(T-BUTYLOXYCARBONYL)-L-HISTIDINE CYCLOHEXYLAMINE
N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-IM-(T-BUTYLOXYCARBONYL)-L-HISTIDINE DICYCLOHEXYLAMINE
N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-IM-(TERT-BUTYLOXYCARBONYL)-L-HISTIDINE DICYCLOHEXYLAMINE
1-[(1,1-Dimethylethoxy)carbonyl]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-histidine compd. with cyclohexanamine
(2S)-3-{1-[(tert-butoxy)carbonyl]-1H-imidazol-4-yl}-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanoic acid
Nα-Fmoc-N(im)-Boc-L-histidine cyclohexylammonium salt, Nim-Boc-Nα-Fmoc-L-histidine cyclohexylammonium salt
L-Histidine, 1-[(1,1-dimethylethoxy)carbonyl]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, compd. with cyclohexanamine (1:1)
[Molecular Formula]

C26H27N3O6.C6H13N
[MDL Number]

MFCD06809743
[MOL File]

210820-99-8.mol
[Molecular Weight]

576.69
Chemical PropertiesBack Directory
[storage temp. ]

−20°C
[form ]

powder
[Major Application]

peptide synthesis
[InChIKey]

UDEXYAHZNOKVIG-FTBISJDPSA-N
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Safety Statements ]

22-24/25
[WGK Germany ]

3
[F ]

10
[HS Code ]

2933 29 90
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

peptide synthesis
[reaction suitability]

reaction type: Fmoc solid-phase peptide synthesis
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