| Identification | Back Directory | [Name]
DIMETHYL ETHYLIDENEMALONATE | [CAS]
17041-60-0 | [Synonyms]
DIMETHYL ETHYLIDENEMALONATE
Dimethyl 2-ethylidenemalonate
Dimethyl ethylidenemalonate 98%
diMethyl 2-ethylidenepropanedioate
Dimethyl 1-propene-1,1-dicarboxylate
Ethylidenemalonic acid dimethyl ester
2-(Ethylidene)malonic acid dimethyl ester
4-hydroxy-1,5-dimethyl-2-phenyl-3-pyrazolone
(Ethylidene)propanedioic acid dimethyl ester
2-Ethylidene-malonic acid 1,3-dimethyl ester
1-Propene-1,1-dicarboxylic acid dimethyl ester
Propanedioic acid, 2-ethylidene-, 1,3-dimethyl ester | [Molecular Formula]
C7H10O4 | [MDL Number]
MFCD00008447 | [MOL File]
17041-60-0.mol | [Molecular Weight]
158.15 |
| Chemical Properties | Back Directory | [Boiling point ]
154℃ | [density ]
1.111 g/mL at 25 °C (lit.) | [refractive index ]
n20/D 1.447(lit.) | [Fp ]
97 °C | [storage temp. ]
Store at room temperature | [Appearance]
Colorless to light yellow Liquid | [InChI]
1S/C7H10O4/c1-4-5(6(8)10-2)7(9)11-3/h4H,1-3H3 | [InChIKey]
FRCFZWCJSXQAMQ-UHFFFAOYSA-N | [SMILES]
COC(=O)\C(=C\C)C(=O)OC |
| Hazard Information | Back Directory | [Uses]
Dimethyl ethylidenemalonate has been employed:
- as electrophile in catalytic asymmetric Michael reactions of enamides and enecarbamates
- in preparation of N-bound α-cyanocarbanion complexes
| [General Description]
Palladium (0)-catalyzed deconjugative allylation of dimethyl ethylidenemalonate has been reported. |
|
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Energy Chemical
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Heterochem
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Sigma-Aldrich
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parabiochem
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Cool Pharm, Ltd
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