Determine the necessary mass, volume, or concentration for preparing a solution.
≥96% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Product Introduction
Palladium (0)-catalyzed deconjugative allylation of dimethyl ethylidenemalonate has been reported.
Application
Dimethyl ethylidenemalonate has been employed:
• as electrophile in catalytic asymmetric Michael reactions of enamides and enecarbamates
• in preparation of N-bound α-cyanocarbanion complexes
| Pubchem Sid | 504759349 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504759349 |
| Sonrisas canónicas | CC=C(C(=O)OC)C(=O)OC |
| IUPAC Name | dimethyl 2-ethylidenepropanedioate |
| InChIKey | FRCFZWCJSXQAMQ-UHFFFAOYSA-N |
| INCHI | 1S/C7H10O4/c1-4-5(6(8)10-2)7(9)11-3/h4H,1-3H3 |
| Isómeros SMILES | CC=C(C(=O)OC)C(=O)OC |
| Peso molecular | 158.15 |
| Reaxy-Rn | 1767127 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1767127&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Clase | Fatty Acyls |
| Subclass | Fatty acid esters |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Fatty acid esters |
| Alternative Parents | Dicarboxylic acids and derivatives Methyl esters Enoate esters Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Fatty acid ester - Dicarboxylic acid or derivatives - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Methyl ester - Carboxylic acid ester - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Sep 26, 2023 | D341726 | |
| Certificate of Analysis | Sep 26, 2023 | D341726 | |
| Certificate of Analysis | Sep 26, 2023 | D341726 | |
| Certificate of Analysis | Sep 26, 2023 | D341726 | |
| Certificate of Analysis | Sep 26, 2023 | D341726 | |
| Certificate of Analysis | Sep 26, 2023 | D341726 |
| Índice de refracción | 1.447 |
|---|---|
| Peso molecular | 158.150 g/mol |
| XLogP3 | 1.000 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 4 |
| Exact Mass | 158.058 Da |
| Monoisotopic Mass | 158.058 Da |
| Topological Polar Surface Area | 52.600 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 175.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |