| Identification | Back Directory | [Name]
H-DL-ASP-OME | [CAS]
65414-77-9 | [Synonyms]
NSC 120023
DL-Asp-OMe
H-DL-ASP-OME
H-Asp(β-OH)-OMe
DL-ASPARTIC ACID-OME
H-DL-ASP-OME USP/EP/BP
DL-Aspartic acid methyl ester
DL-Aspartic acid α-methyl ester
3-amino-4-methoxy-4-oxobutanoicaci
DL-ASPARTIC ACID ALPHA-METHYL ESTER
DL-Aspartic acid α-methyl ester≥ 98% (NMR) | [Molecular Formula]
C5H9NO4 | [MDL Number]
MFCD00237858 | [MOL File]
65414-77-9.mol | [Molecular Weight]
147.13 |
| Chemical Properties | Back Directory | [Boiling point ]
272.7±30.0 °C(Predicted) | [density ]
1.299±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Inert atmosphere,2-8°C | [form ]
solid | [pka]
3.45±0.19(Predicted) | [Appearance]
White to off-white Solid | [Optical Rotation]
3.5°(C=0.156 g/100ml, EA) | [InChI]
1S/C5H9NO4/c1-10-5(9)3(6)2-4(7)8/h3H,2,6H2,1H3,(H,7,8) | [InChIKey]
SWWBMHIMADRNIK-UHFFFAOYSA-N | [SMILES]
COC(=O)C(N)CC(O)=O |
| Hazard Information | Back Directory | [Chemical Properties]
White powder | [Synthesis]
Example 2: 1.75 g of N-formyl-L-aspartic acid α-methyl ester (10 mmol) was dissolved with 3.5 g of hydroxylamine hydrochloride (50 mmol) in 10 mL of 90% methanol solution. The reaction mixture was stirred continuously at 70°C for 4 hours. Upon completion of the reaction, the reaction mixture was confirmed to contain L-aspartic acid α-methyl ester in 85% yield by analysis. | [References]
[1] Patent: US4021418, 1977, A |
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