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Rosuvastatin Impurity 194

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For Research Use Only | Not For Clinical Use
CATAPB01775
Synonyms(3R,5S)-tert-butyl 3,5-dihydroxy-6-((5-methyl-1,3,4-thiadiazol-2-yl)sulfonyl)hexanoate
Molecular Weight366.45
Molecular FormulaC13H22N2O6S2

What is the molecular weight of Rosuvastatin Impurity 194?

The molecular weight of Rosuvastatin Impurity 194 is 366.45.

What is the molecular formula of Rosuvastatin Impurity 194?

The molecular formula of Rosuvastatin Impurity 194 is C13H22N2O6S2.

What are the synonyms for Rosuvastatin Impurity 194?

One of the synonyms is (3R,5S)-tert-butyl 3,5-dihydroxy-6-((5-methyl-1,3,4-thiadiazol-2-yl)sulfonyl)hexanoate.

How many carbon atoms are present in the molecular formula of Rosuvastatin Impurity 194?

There are 13 carbon atoms present in the molecular formula of Rosuvastatin Impurity 194.

What functional groups are present in the molecular formula of Rosuvastatin Impurity 194?

The functional groups present in the molecular formula of Rosuvastatin Impurity 194 are hydroxyl, sulfonyl, and thiadiazol.

What is the molecular structure of Rosuvastatin Impurity 194?

The molecular structure of Rosuvastatin Impurity 194 is (3R,5S)-tert-butyl 3,5-dihydroxy-6-((5-methyl-1,3,4-thiadiazol-2-yl)sulfonyl)hexanoate.

How many oxygen atoms are present in the molecular formula of Rosuvastatin Impurity 194?

There are 6 oxygen atoms present in the molecular formula of Rosuvastatin Impurity 194.

What is the molecular geometry of Rosuvastatin Impurity 194?

The molecular geometry of Rosuvastatin Impurity 194 is determined by the arrangement of atoms and bonds in space.

What is the relevance of Rosuvastatin Impurity 194 in pharmaceutical research?

Rosuvastatin Impurity 194 is important in pharmaceutical research as it is a specific compound that needs to be identified and characterized for quality control purposes.

How is Rosuvastatin Impurity 194 synthesized in a laboratory setting?

Rosuvastatin Impurity 194 can be synthesized in a laboratory setting by following specific chemical reactions and procedures outlined in organic chemistry literature.

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