| Identification | Back Directory | [Name]
FMOC-ASP(OMPE)-OH | [CAS]
180675-08-5 | [Synonyms]
FMOC-ASP(OMPE)-OH
Fmoc-L-Asp(OMpe)-OH
FMOC-ASP(OMPE)-OH 5 G
FMOC-ASPARTIC ACID(OMPE)
FMoc-L-aspartic acid β-Methylpentyl ester
N-Fmoc-L-aspartic acid 4-methylpentyl ester
N-Fmoc-L-asparticacid4-methylpentylester,98%
(9H-Fluoren-9-yl)MethOxy]Carbonyl Asp(OMpe)-OH
N-ALPHA-FMOC-(O-3-METHYL-PENT-3-YL)ASPARTIC ACID
N-Fmoc-L-aspartic Acid 4-(1-Ethyl-1-methylpropyl) Ester
N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-L-ASPARTIC ACID 3-METHYL-PENT-3-YL
N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-L-ASPARTIC ACID 3-METHYLPENTYL ESTER
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-aspartic acid 4-(1-ethyl-1-methylpropyl) ester
L-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 4-(1-ethyl-1-methylpropyl) ester
(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-(3-methylpentan-3-yloxy)-4-oxobutanoic acid
(2S)-4-(1-ethyl-1-methyl-propoxy)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-oxo-butanoic acid
(S)-3-(((9H-fluoren-9-yl)methyl9H-fluoren-9-yl)methoxy)carbonylamino)-4-(3-methylpentan-3-yloxy)-4-oxobutanoic acid | [Molecular Formula]
C28H27NO7 | [MDL Number]
MFCD03424222 | [MOL File]
180675-08-5.mol | [Molecular Weight]
489.52 |
| Chemical Properties | Back Directory | [Boiling point ]
635.9±55.0 °C(Predicted) | [density ]
1.214±0.06 g/cm3(Predicted) | [storage temp. ]
-15°C
| [form ]
Solid | [pka]
3.56±0.23(Predicted) | [Appearance]
White to off-white Solid | [Optical Rotation]
29°(C=0.01g/ml CHCL3) | [Major Application]
peptide synthesis | [InChIKey]
SYGKUYKLHYQKPL-NRFANRHFSA-N | [SMILES]
C(O)(=O)[C@H](CC(OC(CC)(C)CC)=O)NC(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)=O |
| Safety Data | Back Directory | [Symbol(GHS) ]
GHS07 | [Signal word ]
Warning | [Hazard statements ]
H315-H319-H335 | [Precautionary statements ]
P261-P301+P312-P302+P352-P304+P340-P305+P351+P338 | [WGK Germany ]
WGK 2 | [Storage Class]
11 - Combustible Solids |
| Hazard Information | Back Directory | [Description]
The side chain protecting group Mpe in Fmoc-Asp(OMpe)-OH is a more bulky group than the standard tert-Butyl (tBu) group, which significantly helps suppressing the notorious side reaction of aspartimide formation, and thus improve the purity of the crude peptide and facility the time- and cost-intensive purification as well. | [Uses]
FMOC-ASP(OMPE)-OH can be used as organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical production process. | [reaction suitability]
reaction type: Fmoc solid-phase peptide synthesis |
|
| Company Name: |
Shanghai GL Peptide Ltd. Gold
|
| Telephone: |
+86-21-61263310 13764994101 |
| Website: |
www.chemicalbook.com/supplier/10480342/ |
| Company Name: |
Amatek Scientific Co. Ltd. Gold
|
| Telephone: |
0512-56316828 400-867-5858;400-867-5858 |
| Website: |
http://www.amateksci.com |
| Company Name: |
T&W GROUP
|
| Telephone: |
021-61551611 13296011611 |
| Website: |
www.trustwe.com/ |
|