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Diethyl(phenylacetyl)malonate powder Raw Materials CAS 20320-59-6
Product Overview:
Diethyl(phenylacetyl)malonate powder contains two ester bonds, which are relatively low in reactivity, but can be hydrolyzed with the right catalyst to produce compounds such as phenylacetic acid and ethanol. Diethyl(phenylacetyl)malonate CAS 20320-59-6 is an organic synthetic intermediate used in organic chemistry to synthesize heterocyclic compounds.
Diethyl(phenylacetyl)malonate powder Raw Materials CAS 20320-59-6 Attributes
MF:C15H18O5
MW:278.3
EINECS:205-854-1
Specification:Diethyl(phenylacetyl)malonate powder
Sample:Diethyl(phenylacetyl)malonate powder
Brand:Diethyl(phenylacetyl)malonate powder
Appearance: powder
Storage: Cool Dry Place
Brand: chemical Raw Materials
Shelf Life: 2 Years
Test Method: HPLC
Diethyl(phenylacetyl)malonate powder Raw Materials CAS 20320-59-6 Details
Uses and synthesis of Diethyl(phenylacetyl)malonate powder
Diethyl(phenylacetyl)malonate powder contains two ester bonds, which are relatively low in reactivity, but can be hydrolyzed with the right catalyst to produce compounds such as phenylacetic acid and ethanol. Diethyl(phenylacetyl)malonate CAS 20320-59-6 is an organic synthetic intermediate used in organic chemistry to synthesize heterocyclic compounds.
Applications/Functions of Diethyl(phenylacetyl)malonate powder
Diethyl(phenylacetyl)malonate Raw material is an organic synthetic intermediate used in organic chemistry to synthesize heterocyclic compounds.
Physicochemical Property of Diethyl(phenylacetyl)malonate powder
Diethyl(phenylacetyl)malonate powder contains two ester bonds, which are relatively low in reactivity, but can be hydrolyzed with the right catalyst to produce compounds such as phenylacetic acid and ethanol.
Production methodprocess of Diethyl(phenylacetyl)malonate powder
The anhydrous ethanol, which was co-steamed with diethyl phthalate and sodium metal, was added to the mixture of diethyl malonate, carbon tetrachloride and magnesium. The reaction was heated to start and the temperature was controlled to make the reaction smooth.
Then add anhydrous ether, heat for 1h, and add ether solution of phenylacetyl chloride (slowly add, do not make the reaction too intense). After the reaction, the oil layer was separated by cooling and water, and the ether was steamed under reduced pressure to obtain Diethyl(phenylacetyl)malonate CAS 20320-59-6.