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Baloxavir Marboxil Impurity 7

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For Research Use Only | Not For Clinical Use
CATAPB1820001726
CAS1820001-72-6
Synonyms7-fluoro-6,11-dihydrodibenzo[b,e]thiepin-11-ol
Molecular Weight246.3
Molecular FormulaC14H11FOS

What is the chemical name of Baloxavir Marboxil Impurity 7?

The chemical name of Baloxavir Marboxil Impurity 7 is 7-fluoro-6,11-dihydrodibenzo[b,e]thiepin-11-ol.

What is the CAS number of Baloxavir Marboxil Impurity 7?

The CAS number of Baloxavir Marboxil Impurity 7 is 1820001-72-6.

What is the molecular weight of Baloxavir Marboxil Impurity 7?

The molecular weight of Baloxavir Marboxil Impurity 7 is 246.3.

What is the molecular formula of Baloxavir Marboxil Impurity 7?

The molecular formula of Baloxavir Marboxil Impurity 7 is C14H11FOS.

What are the synonyms of Baloxavir Marboxil Impurity 7?

One of the synonyms is 7-fluoro-6,11-dihydrodibenzo[b,e]thiepin-11-ol.

What is the chemical structure of Baloxavir Marboxil Impurity 7?

The chemical structure of Baloxavir Marboxil Impurity 7 is a dibenzo[b,e]thiepin ring with a fluorine atom at position 7 and a hydroxyl group at position 11.

Why is it important to identify and characterize impurities in pharmaceutical products?

It is important to identify and characterize impurities in pharmaceutical products to ensure safety, efficacy, and quality of the drug for patient consumption.

How is Baloxavir Marboxil Impurity 7 produced during the manufacturing process?

Baloxavir Marboxil Impurity 7 may be produced as a byproduct or degradation product during the synthesis of Baloxavir Marboxil.

What potential risks could Baloxavir Marboxil Impurity 7 pose to patients if present in the drug product?

Baloxavir Marboxil Impurity 7 could potentially pose risks such as reduced efficacy, increased toxicity, or adverse reactions in patients if present in the drug product.

How can Baloxavir Marboxil Impurity 7 be controlled or minimized in the manufacturing process?

Baloxavir Marboxil Impurity 7 can be controlled or minimized by optimizing the synthesis process, implementing purification steps, and monitoring impurity levels through quality control testing.

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