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Elagolix Impurity 24

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For Research Use Only | Not For Clinical Use
CATAPB05831
Synonyms5-chloro-1-(2-fluoro-6-(trifluoromethyl)benzyl)-6-methylpyrimidine-2,4(1H,3H)-dione
Molecular Weight336.67
Molecular FormulaC13H9ClF4N2O2

What is the product name of Elagolix Impurity 24?

The product name of Elagolix Impurity 24 is 5-chloro-1-(2-fluoro-6-(trifluoromethyl)benzyl)-6-methylpyrimidine-2,4(1H,3H)-dione.

What is the synonym for Elagolix Impurity 24?

The synonym for Elagolix Impurity 24 is 5-chloro-1-(2-fluoro-6-(trifluoromethyl)benzyl)-6-methylpyrimidine-2,4(1H,3H)-dione.

What is the molecular weight of Elagolix Impurity 24?

The molecular weight of Elagolix Impurity 24 is 336.67.

What is the molecular formula of Elagolix Impurity 24?

The molecular formula of Elagolix Impurity 24 is C13H9ClF4N2O2.

What is the chemical structure of Elagolix Impurity 24?

The chemical structure of Elagolix Impurity 24 is a pyrimidine ring with chloro, fluoro, methyl, and trifluoromethyl substituents.

How many fluorine atoms are present in the molecular formula of Elagolix Impurity 24?

There are four fluorine atoms present in the molecular formula of Elagolix Impurity 24.

What is the role of Elagolix Impurity 24 in pharmaceutical research?

Elagolix Impurity 24 may serve as a reference material or standard in pharmaceutical research for quality control and analytical testing purposes.

How is Elagolix Impurity 24 synthesized in the laboratory?

Elagolix Impurity 24 can be synthesized by a series of chemical reactions involving fluorination, chlorination, and methyl substitution on a pyrimidine scaffold.

What are the potential chemical reactions involving Elagolix Impurity 24 in pharmacological studies?

Elagolix Impurity 24 may undergo metabolism, degradation, or interaction with other drug compounds in pharmacological studies, leading to the formation of new chemical entities or impurities.

How can Elagolix Impurity 24 be characterized and identified in pharmaceutical formulations?

Elagolix Impurity 24 can be characterized and identified by various analytical techniques such as mass spectrometry, nuclear magnetic resonance spectroscopy, and high-performance liquid chromatography.

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