Buy Diethyl (phenylacetyl)malonate Cas 20320-59-6
Buy Diethyl (phenylacetyl)malonate Cas 20320-59-6
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Cas 20320-59-6
new bmk 20320-59-6
Diethyl(phenylacetyl)malonate
2-(2-phenylacetyl)propanedioate
Diethyl(phenylacetyl)malonate(new bmk)
phenylacetyl-malonic acid diethyl ester
White Powder New P Pharmaceutical Grade
diethyl 2-(2-phenylacetyl)propanedioate
diethyl 2-(2-phenylacetyl)propanedioatec
White Powder Diethyl(phenylacetyl)malonate
Diethyl(phenylacetyl)malonate White Powder
Propanedioic acid, (phenylacetyl)-, diethyl ester
Diethyl 2-(2-phenylacetyl)propanedioate 99% Purity
diethyl 2-(2-phenylacetyl)propanedioate wickr bettyml
Propanedioic acid, 2-(2-phenylacetyl)-, 1,3-diethyl ester
Pharmaceutical intermediates Diethyl(phenylacetyl)malonate
Diethyl 2-(2-phenylacetyl)propanedioate Pharmaceutical Grade
High Purity Propanedioic acid, 2-(2-phenylacetyl)-, 1,3-diethyl ester
| [EINECS(EC#)]
205-854-1 |
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| [Molecular Formula]
C15H18O5 |
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| [MDL Number]
MFCD28989869 |
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| [MOL File] | |
| [Molecular Weight]
278.3 |
| Chemical Properties | Back Directory |
| [Boiling point ]
120 °C(Press: 0.01 Torr) |
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| [density ]
1.148±0.06 g/cm3(Predicted) |
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| [form ]
Brown liquid |
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| [pka]
8.76±0.59(Predicted) |
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| [InChI]
InChI=1S/C15H18O5/c1-3-19-14(17)13(15(18)20-4-2)12(16)10-11-8-6-5-7-9-11/h5-9,13H,3-4,10H2,1-2H3 |
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| [InChIKey]
ZASPDQDIPTZTQQ-UHFFFAOYSA-N |
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| [SMILES]
C(OCC)(=O)C(C(CC1=CC=CC=C1)=O)C(OCC)=O |
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| Raw materials And Preparation Products | Back Directory |
| Hazard Information | Back Directory | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| [Physical properties]
Diethyl(phenylacetyl)malonate has a boiling point of 120 °C. Its density is predicted to be 1.148±0.06 g/cm3. |
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| [Uses]
Organic synthesis intermediates. |
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| [Preparation]
The anhydrous ethanol co-vaporized with diethyl phthalate and sodium metal is added dropwise to the mixture of diethyl malonate, carbon tetrachloride and magnesium, heated to start the reaction, and the temperature is controlled to smooth the reaction. Then add anhydrous diethyl ether, heat for 1h, add the diethyl ether solution of phenylacetyl chloride (add slowly, not to make the reaction too intense). After the reaction is completed, cool and add water, separate the oil layer, and evaporate the diethyl ether under reduced pressure to obtain diethyl(phenylacetyl)malonate. |
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| [storage]
Dry and cool place and keep away from strong light.
Diethyl(phenylacetyl)malonate Another name：phenylacetyl-malonic acid diethyl ester;Phenylacetyl-malonsaeure-diaethylester;Phenylacetylmalonsaeurediethylester; CasNo: 20320-59-6 Purity： ≥98% Molecular Structure： C15H18O5
Diethyl(phenylacetyl)malonate Basic Product Information Product NameCASSynonymsMolecular FormulaEINECS NumberMolecular StructureAppearance PuritySupply Ability
Diethyl(phenylacetyl)malonate Quality documents Diethyl(phenylacetyl)malonate Appearance/Package/Shipping/Storage Package 25kg/drum Storage condition Store in a cool, dry, and sealed place； Diethyl(phenylacetyl)malonate Application Organic synthesis intermediates, pharmaceutical intermediates; Diethyl(phenylacetyl)malonate literature Comprehensive study on excited state intramolecular proton transfer in 2-(benzo[d]thiazol-2-yl)-3-methoxynaphthalen-1-ol and 2-(benzo[d]thiazol-2-yl)naphthalene-1,3-diol: Effect of solvent, aggregation, viscosity and TDDFT study Warde, Umesh,Nagaiyan, Sekar , p. 33 – 43 (2017) Three compounds DMT, MMT and DHT having dimehtoxy, mono-hydroxy and di-hydroxy groups respectively were prepared. Environmental interactions dependent photophysical properties especially excited state intramolecular proton transfer (ESIPT), solvatochromism, aggregation induced emission enhancement (AIEE) and viscosity dependent emission characteristics were studied. The effect of solvent polarity on ESIPT dynamics were studied using UV–vis and emission spectroscopy along with aggregation induced enhanced emission and viscosity effect. MMT and DHT showed unexpected and contrasting behavior in the solvents which are in good agreement with the density functional theory and time dependent density functional theory findings. Aggregation and viscosity study showed that cis-keto emission increased drastically in the aggregate state and highly viscous state due to restricted intramolecular rotation increasing the population of required cis enol rotamer (E). The study directs the potential applications of such molecules for advanced optoelectronics and viscosity based investigations. The Interrupted Pummerer Reaction in a Sulfoxide-Catalyzed Oxidative Coupling of 2-Naphthols He, Zhen,Pulis, Alexander P.,Procter, David J. supporting information, p. 7813 – 7817 (2019/05/15) A benzothiophene S-oxide catalyst, generated in situ by sulfur oxidation with H2O2, mediates the oxidative coupling of 2-naphthols. Key to the catalytic process is the capture and inversion of reactivity of a 2-naphthol partner, using an interrupted Pummerer reaction of an unusual benzothiophene S-oxide, followed by subsequent coupling with a second partner. The new catalytic manifold has been showcased in the synthesis of the bioactive natural products, (±)-nigerone and (±)-isonigerone. Although Pummerer reactions are used widely, their application in catalysis is rare, and our approach represents a new catalytic manifold for metal-free C?C bond formation. INDOLIN-2-ONE DERIVATIVES AS PROTEIN KINASE INHIBITORS – , (2013/11/05) A novel class of indoline-2-one derivatives are disclosed. These compounds are protein kinase inhibitors which are useful for treating hyperproliferative diseases such as cancer. Novel Inhibitors of Hepatitis C Virus Replication – Page/Page column 52-53, (2009/10/21) The embodiments provide compounds of the general Formula I, as well as compositions, including pharmaceutical compositions, comprising a subject compound. The embodiments further provide treatment methods, including methods of treating a hepatitis C virus infection and methods of treating liver fibrosis, the methods generally involving administering to an individual in need thereof an effective amount of a subject compound or composition. Diethyl(phenylacetyl)malonate Upstream and downstream 20320-59-6 Upstream product
Buy Diethyl(phenylacetyl)malonate Diethyl(phenylacetyl)malonate, also known as diethyl phenylacetylmalonate, is an organic compound classified as a complex ester. This compound is a derivative of malonic acid where one of the hydrogens is replaced by a phenylacetyl group. Synonyms: Diethyl 2-(2-phenylacetyl)propanedioate Key Features:
Applications:Diethyl(phenylacetyl)malonate is used in organic synthesis, predominantly as a precursor or reagent in the synthesis of various chemical compounds. It can be used to create a variety of pharmaceutical products, including active pharmaceutical ingredients. This compound can also play a role in the synthesis of peptides and other complex organic molecules, including narcotic analogs, making it an important component in chemical research. Additional Information Not for food, drug, human, animal or household use. For laboratory, R&D, industrial or manufacturing only.
Diethyl(phenylacetyl)malonate
Last updated:2026-03-01 21:15:31
Diethyl(phenylacetyl)malonate Chemical Properties, Uses, ProductionChemical PropertiesDiethyl phenylacetylmalonate contains two ester bonds, which are relatively unreactive, but which can be hydrolyzed in the presence of a suitable catalyst to produce compounds such as phenylacetic acid and ethanol. The compound can also be esterified with other alcohols to produce different ester compounds, e.g., with methanol to give methyl phenylacetylmalonate. By acid-catalyzed hydrolysis, the compound can generate phenylacetylmalonic acid, and further addition of water can obtain phenylacetic acid and diethyl malonate. Physical propertiesDiethyl(phenylacetyl)malonate has a boiling point of 120 °C. Its density is predicted to be 1.148±0.06 g/cm3. UsesOrganic synthesis intermediates. PreparationThe anhydrous ethanol co-vaporized with diethyl phthalate and sodium metal is added dropwise to the mixture of diethyl malonate, carbon tetrachloride and magnesium, heated to start the reaction, and the temperature is controlled to smooth the reaction. Then add anhydrous diethyl ether, heat for 1h, add the diethyl ether solution of phenylacetyl chloride (add slowly, not to make the reaction too intense). After the reaction is completed, cool and add water, separate the oil layer, and evaporate the diethyl ether under reduced pressure to obtain diethyl(phenylacetyl)malonate. storageDry and cool place and keep away from strong light.    Synthesis of Diethyl(phenylacetyl)malonate from Ethanol and 1,3-Dioxane-4,6-dione, 2,2-dimethyl-5-(2-phenylacetyl)-
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Diethyl(phenylacetyl)malonate Propanedioic acid, 2-(2-phenylacetyl)-, 1,3-diethyl ester Propanedioic acid, (phenylacetyl)-, diethyl ester Pharmaceutical intermediates Diethyl(phenylacetyl)malonate 2-(2-phenylacetyl)propanedioate White Powder New P Pharmaceutical Grade Diethyl(phenylacetyl)malonate White Powder White Powder Diethyl(phenylacetyl)malonate High Purity Propanedioic acid, 2-(2-phenylacetyl)-, 1,3-diethyl ester Diethyl 2-(2-phenylacetyl)propanedioate Pharmaceutical Grade diethyl 2-(2-phenylacetyl)propanedioatec phenylacetyl-malonic acid diethyl ester Diethyl 2-(2-phenylacetyl)propanedioate 99% Purity new bmk 20320-59-6 Diethyl(phenylacetyl)malonate(new bmk) bmk Lliquid oil New BMK Oil New BMK Oil Diethyl(phenylacetyl)malonate bmk oil wickr:bellakmbk Diethyl(phenylacetyl)malonate china Diethyl(phenylacetyl)malonate stocks Diethyl(phenylacetyl)malonate large stock Diethyl(phenylacetyl)malonate (New BMK oil ) Diethyl(phenylacetyl)malonate bmk oil pmk oil phenylacetyl)malonate, new bmk oil Pharmaceutical Intermediate BMK OIL diethyl 2-(2-phenylacetyl)propanedioate wickr bettyml diethyl 2-(2-phenylacetyl)propanedioate new p Propanedioic Phenylacetylmalonsaeurediethylester 20320 59 6 Diethyl(phenylacetyl)malonate(BMK Oil) Phenylacetylmalonic acid ethylester Diethyl(phenylacetyl)malonate(BMK) iethyl2-(2-phenylacetyl)propanedioate BMK Oil/powder Diethyi(phenylacetyl)malonate BMK Glycidic Acid Diethyl(phenylacetyl)malonate Diethyl(phenylacetyl)malonate,new bmk 20320-59-6 Wickr jane8886 BMK Diethyl(phenylacetyl)malonate Pharmaceutical intermediates Diethyl(phenylacetyl) Diethyl(phenylacetyl)malonate Oil Powder BMK Oil Diethyl( phenylacetyl) Malonate Cas 20320-59-6 20320-59-6 288573-93-9 20320-59-9 20320-59-6 BMK
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Diethyl (phenylacetyl)malonate | 20320-59-6 – ChemicalBook
Mar 1, 2026 · Diethyl (phenylacetyl)malonate (CAS 20320-59-6) information, including chemical properties, structure, melting point, …
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Diethyl phenylacetyl malonate is an organic synthesis intermediate used in the synthesis of fine chemicals and active pharmaceutical …
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Diethyl (phenylacetyl)malonate | CAS#:20320-59-6 | Chemsrc
Jul 1, 2026 · Chemsrc provides Diethyl (phenylacetyl)malonate (CAS#:20320-59-6) MSDS, density, melting point, boiling point, …
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Molecular Formula: C 15 H 18 O 5
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Name: diethyl 2- (2-phenylacetyl)propanedioate
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Molecular Weight: 278.30000
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Diethyl (phenylacetyl)malonate – Ozon Chemical
Diethyl (phenylacetyl)malonate is used in organic synthesis, predominantly as a …
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CAS number: 20320-59-6
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Molar mass: 278.3 g/mol
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Formula: C15H18O5
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Buy-CAS 20320-59-6 Diethyl (phenylacetyl)malonate20320-59-6
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