Place of Origin: | China |
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Brand Name: | First |
Certification: | COA |
Model Number: | 20320-59-6 |
Minimum Order Quantity: | 1kg |
Price: | 50-100 USD /KG |
Packaging Details: | 1kg/bag ;25kg/drum,25 kg/Carton |
Delivery Time: | 5-10 work days |
Payment Terms: | T/T, Western Union, MoneyGram |
Supply Ability: | 1000 Tons |
CAS: | 20320-59-6 | Product Name: | BMK Methyl Glycidate CAS 20320-59-6 Diethyl(Phenylacetyl)Malonate C15H18O5 |
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MF: | 206.24 | Type: | Syntheses Material Intermediates |
Appearance: | White Bmk Powder | ||
High Light: | BMK Glycidate Powder CAS 20320-59-6, CAS 20320-59-6, Diethyl(Phenylacetyl)Malonate |
Product Name: | Diethyl(phenylacetyl)malonate |
Synonyms: | Diethyl(phenylacetyl)malonate;Propanedioic acid, 2-(2-phenylacetyl)-, 1,3-diethyl ester;diethyl 2-(2-phenylacetyl)propanedioate;diethyl 2-(2-phenylacetyl)propanedioate wickr bettyml;Cas 20320-59-6;Propanedioic acid, (phenylacetyl)-, diethyl ester;Pharmaceutical intermediates Diethyl(phenylacetyl)malonate;new p |
CAS: | 20320-59-6 |
MF: | C15H18O5 |
MW: | 278.3 |
EINECS: | 205-854-1 |
Product Categories: | 20320-59-6;BMK |
Mol File: | 20320-59-6.mol |
Boiling point | 120 °C(Press: 0.01 Torr) |
density | 1.148±0.06 g/cm3(Predicted) |
pka | 8.76±0.59(Predicted) |
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 |
InChIKey | ZASPDQDIPTZTQQ-UHFFFAOYSA-N |
SMILES | C(OCC)(=O)C(C(CC1=CC=CC=C1)=O)C(OCC)=O |
Physical properties | Diethyl(phenylacetyl)malonate has a boiling point of 120 °C. Its density is predicted to be 1.148±0.06 g/cm3. |
Uses | Organic synthesis intermediates. |
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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