2,2,14,14-Tetramethyl-8-oxopentadecanedioic acid diethyl ester is the diethyl ester derivative of 2,2,14,14-tetramethyl-8-oxopentadecanedioic acid. The esterification of the terminal carboxylic acids increases its lipophilicity and volatility, making it an ideal precursor for specialized synthetic applications.
Mechanism of Action
It acts as a protected, lipid-soluble building block. The ethyl ester groups allow for better penetration in certain chemical processes, and can be selectively hydrolyzed to reveal the active diacid. The core structure maintains the metabolic stability provided by the gem-dimethyl groups.
Application
It is primarily used as an intermediate in the synthesis of macrocyclic compounds and as a specialized reagent in the development of novel lipid-regulating pharmaceuticals.
How does 2,2,14,14-Tetramethyl-8-oxopentadecanedioic acid diethyl ester differ from the acid?
The ester form of it offers increased lipophilicity and different solubility profiles.
Is 2,2,14,14-Tetramethyl-8-oxopentadecanedioic acid diethyl ester stable?
Yes, it is chemically stable when stored under recommended conditions.
What is the application of 2,2,14,14-Tetramethyl-8-oxopentadecanedioic acid diethyl ester?
It is used as a precursor for macrocyclic drugs and metabolic research.
Is 2,2,14,14-Tetramethyl-8-oxopentadecanedioic acid diethyl ester produced under industry standards?
Yes, its manufacturing follows international standards for high-purity intermediates.
Are technical docs provided for 2,2,14,14-Tetramethyl-8-oxopentadecanedioic acid diethyl ester?
Yes, a COA and SDS are provided for it upon request.