ethyl 2-oxo-2-(1-oxo-3,4-dihydro-2H-naphthalen-2-yl)acetate


Chemical Name: ethyl 2-oxo-2-(1-oxo-3,4-dihydro-2H-naphthalen-2-yl)acetate
CAS Number: 58199-07-8
Product Number: AG00JSUC(AGN-PC-0NIH93)
Synonyms:
MDL No:
Molecular Formula: C14H14O4
Molecular Weight: 246.2586

Identification/Properties


Safety Information


GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum


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Chemical Structure



Ethyl 2-oxo-2-(1-oxo-1,2,3,4-tetrahydronaphthalen-2-yl)acetate is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in the preparation of various organic molecules. Its unique structure containing both a ketone and an ester functional group makes it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals.In chemical synthesis, Ethyl 2-oxo-2-(1-oxo-1,2,3,4-tetrahydronaphthalen-2-yl)acetate can participate in a variety of reactions such as condensations, reductions, and functional group transformations. It can undergo acylation or alkylation reactions to introduce new functional groups, leading to the formation of complex molecular scaffolds. Additionally, this compound can be utilized in the synthesis of heterocyclic compounds and natural product derivatives.The application of Ethyl 2-oxo-2-(1-oxo-1,2,3,4-tetrahydronaphthalen-2-yl)acetate in chemical synthesis enables chemists to access structurally diverse compounds with potential biological activities. Its versatility and reactivity make it a valuable tool for designing and preparing novel molecules for various industrial and research applications.