CasNo： 20320-59-6
Molecular Formula： C15H18O5
Diethyl(phenylacetyl)malonate has a malonate core, with two ethyl groups attached to one of the malonate carbon atoms. The other malonate carbon is part of the phenylacetyl substituent, which includes a phenyl group and an acetyl group.. We supply high quality Diethyl(phenylacetyl)malonate (CAS 20320-59-6), in stock, factory directly supply to clients, lower prices, more competitiveness.
Diethyl(phenylacetyl)malonate is a chemical compound used in the synthesis of barbiturates, particularly phenobarbital, while it's Molecular Formula is C15H18O5. Organic synthesis intermediates.
The CAS number of Diethyl(phenylacetyl)malonate is 20320-59-6.
More information of Diethyl(phenylacetyl)malonate 20320-59-6 are:
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Synonyms |
phenylacetyl-malonic acid diethyl ester;Phenylacetyl-malonsaeure-diaethylester;Phenylacetylmalonsaeurediethylester;Phenylacetylmalonic acid ethylester; |
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CAS Number |
20320-59-6 |
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Molecular Formula |
C15H18O5 |
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Molecular Weight |
278.305 |
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Density |
1.148±0.06 g/cm3(Predicted) |
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Boiling Point |
120 °C(Press: 0.01 Torr) |
| DSSTox Substance ID | DTXSID30447383 |
| Wikidata | Q82266248 |
| Heavy Atom Count | 20 |
| Complexity | 326 |
Synthesis of Barbiturates: Used in the synthesis of barbiturates, such as phenobarbital.
Medicinal Compounds: Diethyl malonate, a related compound, is used in the production of various medicinal compounds, including vigabatrin, phenylbutazone, nalidixic acid, and rebamipide.
Pesticides: Used in the production of pesticides like sethoxydim and derivatives of 2-amino-4-chloro-6-methoxypyrimidine.
Other Applications: Diethyl malonate is employed in washing and cleaning products, coating products, laboratory chemicals, pharmaceuticals, adhesives and sealants, and as pH regulators and water treatment products.
Articles related to Diethyl(phenylacetyl)malonate:
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Article |
Source |
| Kinetics and mechanism of the stepwise dissociation of iron (III) from ferrioxamine B in aqueous acid |
B Monzyk, AL Crumbliss , Journal of the american chemical society, 1982 Then the anion of dimethyl malonate (6 mmol) in 12 mL of THF was added at 25 C under CO to give a light red solution immediately. The red color faded into light amber (~5 min). |
| Heterocyclic compounds: Part XI. Synthetic experiments in the quinazoline series |
M Krishnan , Proceedings of the Indian Academy of Sciences, 1958 The unsuccessful attempts of Bogert and co-workers to cyclise acetyl, phenylacetyl and … derivative of phenyl diethyl malonate, yielding o-nitrobenzoyl-phenyl diethyl malonate. |
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