| Identification | More | [Name]
Fmoc-N-methyl-L-aspartic acid 4-tert-butyl ester | [CAS]
152548-66-8 | [Synonyms]
FMOC-L-MEASP(TBU)-OH
FMOC-MEASP(OTBU)-OH
FMOC-N-ALPHA-METHYL-L-ASPARTIC ACID BETA-T-BUTYL ESTER
FMOC-N-ME-ASPARTIC ACID(OTBU)-OH
FMOC-N-ME-ASP(OTBU)-OH
FMOC-N-METHYL-L-ASPARTIC ACID BETA-T-BUTYL ESTER
N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-N-ALPHA-METHYL-L-ASPARTIC ACID BETA-T BUTYL ESTER
N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-ALPHA-METHYL-L-ASPARTIC ACID BETA-TERT-BUTYL ESTER
N-ALPHA-FMOC-N-ALPHA-METHYL-L-ASPARTIC ACID BETA-T-BUTYL ESTER
FMOC-N-ME-ASP(OBUT)-OH
N-alpha-(9-Fluorenylmethyloxycarbonyl)-N-alpha-methyl-L-aspartic acid beta-t-butyl ester
Fmoc-N-methyl-L-aspartic acid 4-tert-butyl ester
N-(9-Fluorenylmethyloxycarbonyl)-N-methyl-L-aspartic acid 4-tert-butyl ester | [EINECS(EC#)]
240-880-5 | [Molecular Formula]
C24H27NO6 | [MDL Number]
MFCD00237027 | [Molecular Weight]
425.47 | [MOL File]
152548-66-8.mol |
| Chemical Properties | Back Directory | [Melting point ]
135-140°C | [Boiling point ]
598.7±50.0 °C(Predicted) | [density ]
1.237±0.06 g/cm3(Predicted) | [storage temp. ]
-15°C | [solubility ]
Soluble in water or 1% acetic acid | [form ]
Powder | [pka]
3.59±0.23(Predicted) | [color ]
White to off-white | [Optical Rotation]
[α]22/D -39.0°, c = 0.5% in DMF | [Major Application]
peptide synthesis | [InChI]
InChI=1S/C24H27NO6/c1-24(2,3)31-21(26)13-20(22(27)28)25(4)23(29)30-14-19-17-11-7-5-9-15(17)16-10-6-8-12-18(16)19/h5-12,19-20H,13-14H2,1-4H3,(H,27,28)/t20-/m0/s1 | [InChIKey]
CYWWLVIEAOUXGW-FQEVSTJZSA-N | [SMILES]
C(O)(=O)[C@H](CC(OC(C)(C)C)=O)N(C(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)=O)C | [CAS DataBase Reference]
152548-66-8(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
N | [Risk Statements ]
50/53 | [Safety Statements ]
60-61 | [WGK Germany ]
3 | [HS Code ]
2924 29 70 | [HazardClass ]
IRRITANT | [Storage Class]
11 - Combustible Solids |
| Hazard Information | Back Directory | [Chemical Properties]
White to off-white solid | [Uses]
Fmoc protected N-methyl amino acid suitable for solid phase peptide synthesis. N-methyl amino acids have been shown to improve proteolytic stability of peptides. | [reaction suitability]
reaction type: Fmoc solid-phase peptide synthesis |
|
|