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Rivaroxaban iMpurity is a chemical impurity associated with the anticoagulant drug rivaroxaban. It is a potential impurity that can be present in rivaroxaban drug substances, which may impact the quality, safety, and efficacy of the drug. The detection and quantification of Rivaroxaban iMpurity are crucial in the development and production of rivaroxaban drug products to ensure compliance with regulatory requirements and maintain the safety and efficacy of the medication.

1616563-62-2

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1616563-62-2 Usage

Uses

Used in Pharmaceutical Industry:
Rivaroxaban iMpurity is used as a quality control parameter for ensuring the purity and safety of rivaroxaban drug products. It is essential to monitor and control the presence of this impurity to comply with regulatory requirements and guarantee the efficacy and safety of the medication.
Used in Drug Development:
Rivaroxaban iMpurity is utilized as a critical parameter in the development of rivaroxaban drug products. Detecting and quantifying the impurity helps in optimizing the manufacturing process and ensuring the quality of the final product.
Used in Regulatory Compliance:
Rivaroxaban iMpurity serves as a key factor in meeting regulatory requirements for the production and distribution of rivaroxaban drug products. Monitoring its presence ensures that the medication adheres to the necessary safety and efficacy standards.

Check Digit Verification of cas no

The CAS Registry Mumber 1616563-62-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,6,5,6 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1616563-62:
(9*1)+(8*6)+(7*1)+(6*6)+(5*5)+(4*6)+(3*3)+(2*6)+(1*2)=172
172 % 10 = 2
So 1616563-62-2 is a valid CAS Registry Number.

1616563-62-2Downstream Products

1616563-62-2Relevant articles and documents

RIVAROXABAN INTERMEDIATE AND PREPARATION THEREOF

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, (2014/07/21)

This invention relates to novel intermediate, formula (A) for rivaroxaban and process for the preparation thereof. Further it extends to the process for preparation of rivaroxaban by using the said novel intermediate, by treating with 5-chlorothiophene carbonyl chloride to form the rivaroxaban derivatives of formula (B). The obtained formula (B) further treated with acid to form rivaroxaban.

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