Faroenem Impurity 16

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For Research Use Only | Not For Clinical Use

CAT	APB06349
Synonyms	(5R,6S)-6-((R)-1-hydroxyethyl)-7-oxo-3-((R)-tetrahydrofuran-2-yl)-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid 4-oxide
Molecular Weight	301.32
Molecular Formula	C12H15NO6S

What is the synonym for Faroenem Impurity 16?

The synonym for Faroenem Impurity 16 is (5R,6S)-6-((R)-1-hydroxyethyl)-7-oxo-3-((R)-tetrahydrofuran-2-yl)-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid 4-oxide.

What is the molecular weight of Faroenem Impurity 16?

The molecular weight of Faroenem Impurity 16 is 301.32.

What is the molecular formula of Faroenem Impurity 16?

The molecular formula of Faroenem Impurity 16 is C12H15NO6S.

What are the chemical elements present in the molecular formula of Faroenem Impurity 16?

The chemical elements present in the molecular formula of Faroenem Impurity 16 are carbon, hydrogen, nitrogen, oxygen, and sulfur.

How many carbon atoms are there in the molecular formula of Faroenem Impurity 16?

There are 12 carbon atoms in the molecular formula of Faroenem Impurity 16.

What is the molecular structure of Faroenem Impurity 16?

The molecular structure of Faroenem Impurity 16 is 3D and complex due to the presence of multiple functional groups.

Are there any known uses for Faroenem Impurity 16 in the pharmaceutical industry?

Faroenem Impurity 16 is primarily used as a reference standard for analysis and quality control purposes in the pharmaceutical industry.

How is Faroenem Impurity 16 typically synthesized in the laboratory?

Faroenem Impurity 16 can be synthesized through a series of organic reactions involving the appropriate starting materials and reagents under controlled conditions.

What is the significance of identifying and characterizing impurities like Faroenem Impurity 16 in pharmaceutical products?

Identifying and characterizing impurities like Faroenem Impurity 16 is crucial for ensuring the safety, efficacy, and quality of pharmaceutical products, as impurities can affect the stability and performance of the final drug product.

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