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200616-40-6

200616-40-6 Structure

200616-40-6 Structure
IdentificationMore
[Name]

Fmoc-N-methyl-L-glutamic acid 5-tert-butyl ester
[CAS]

200616-40-6
[Synonyms]

FMOC-L-MEGLU(TBU)-OH
FMOC-MEGLU(OTBU)-OH
FMOC-N-ALPHA-METHYL-L-GLUTAMIC ACID GAMMA-T-BUTYL ESTER
FMOC-N-ME-GLU(OTBU)-OH
FMOC-N-ME-GLUTAMIC ACID(OTBU)-OH
FMOC-N-METHYL-L-GLUTAMIC ACID-GAMMA-T-BUTYL ESTER
N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-N-ALPHA-METHYL-L-GLUTAMIC ACID GAMMA-T-BUTYL ESTER
N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-ALPHA-METHYL-L-GLUTAMIC-ACID-GAMMA-T-BUTYL ESTER
N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-ALPHA-METHYL-L-GLUTAMIC-ACID-GAMMA-TERT-BUTYL ESTER
N-ALPHA-FMOC-N-ALPHA-METHYL-L-GLUTAMIC ACID GAMMA-T-BUTYL ESTER
Fmoc-N-methyl-L-glutamic acid 5-tert-butyl ester
N-(9-Fluorenylmethyloxycarbonyl)-N-methyl-L-glutamic acid 5-tert-butyl ester
[Molecular Formula]

C25H29NO6
[MDL Number]

MFCD00237028
[Molecular Weight]

439.5
[MOL File]

200616-40-6.mol
Chemical PropertiesBack Directory
[Melting point ]

116-119°C
[Boiling point ]

612.3±55.0 °C(Predicted)
[density ]

1.220±0.06 g/cm3(Predicted)
[storage temp. ]

-15°C
[solubility ]

Soluble in water or 1% acetic acid
[form ]

Powder
[pka]

3.72±0.10(Predicted)
[color ]

White to off-white
[Major Application]

peptide synthesis
[InChI]

1S/C25H29NO6/c1-25(2,3)32-22(27)14-13-21(23(28)29)26(4)24(30)31-15-20-18-11-7-5-9-16(18)17-10-6-8-12-19(17)20/h5-12,20-21H,13-15H2,1-4H3,(H,28,29)/t21-/m0/s1
[InChIKey]

FVUASVBQADLDRO-NRFANRHFSA-N
[SMILES]

C(O)(=O)[C@H](CCC(OC(C)(C)C)=O)N(C(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)=O)C
[CAS DataBase Reference]

200616-40-6(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Environment (GHS09)
GHS09
[Signal word ]

Warning
[Hazard statements ]

H410
[Precautionary statements ]

P273-P391-P501
[Hazard Codes ]

N
[Risk Statements ]

50/53
[Safety Statements ]

60-61
[WGK Germany ]

3
[HazardClass ]

IRRITANT
[HS Code ]

2924297099
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Chemical Properties]

White to off-white powder
[Uses]

Fmoc-protected N-methyl amino acid. N-methyl amino acids have shown enhanced biological stability in peptides compared to standard amino acids.
[reaction suitability]

reaction type: Fmoc solid-phase peptide synthesis
Spectrum DetailBack Directory
[Spectrum Detail]

Fmoc-N-methyl-L-glutamic acid 5-tert-butyl ester(200616-40-6)1HNMR
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