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Cabotegravir Impurity 4

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For Research Use Only | Not For Clinical Use
CATAPB05058
Synonyms(3S,11aS)-6-methoxy-3-methyl-5,7-dioxo-2,3,5,7,11,11a-hexahydrooxazolo[3,2-a]pyrido[1,2-d]pyrazine-8-carboxylic acid
Molecular Weight294.09
Molecular FormulaC13H14N2O6

What is the product name of Cabotegravir Impurity 4?

The product name of Cabotegravir Impurity 4 is Cabotegravir Impurity 4.

What is the synonym for Cabotegravir Impurity 4?

The synonym for Cabotegravir Impurity 4 is (3S,11aS)-6-methoxy-3-methyl-5,7-dioxo-2,3,5,7,11,11a-hexahydrooxazolo[3,2-a]pyrido[1,2-d]pyrazine-8-carboxylic acid.

What is the molecular weight of Cabotegravir Impurity 4?

The molecular weight of Cabotegravir Impurity 4 is 294.09.

What is the molecular formula of Cabotegravir Impurity 4?

The molecular formula of Cabotegravir Impurity 4 is C13H14N2O6.

What is the chemical structure of Cabotegravir Impurity 4?

The chemical structure of Cabotegravir Impurity 4 is (3S,11aS)-6-methoxy-3-methyl-5,7-dioxo-2,3,5,7,11,11a-hexahydrooxazolo[3,2-a]pyrido[1,2-d]pyrazine-8-carboxylic acid.

How many carbon atoms are present in the molecular formula of Cabotegravir Impurity 4?

There are 13 carbon atoms present in the molecular formula of Cabotegravir Impurity 4.

What is the total number of atoms in the molecular formula of Cabotegravir Impurity 4?

The total number of atoms in the molecular formula of Cabotegravir Impurity 4 is 35.

What functional groups are present in the chemical structure of Cabotegravir Impurity 4?

The functional groups present in the chemical structure of Cabotegravir Impurity 4 are carboxylic acid and oxazolo.

How is Cabotegravir Impurity 4 used in pharmaceutical research?

Cabotegravir Impurity 4 is used as a reference standard in pharmaceutical research for quality control and analytical purposes.

What is the significance of identifying and characterizing Cabotegravir Impurity 4 in drug development?

Identifying and characterizing Cabotegravir Impurity 4 is crucial in drug development to ensure the safety, efficacy, and quality of the final drug product.

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