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Dabigatran iMpurity E is a chemical compound that is classified as an impurity of the anticoagulant drug Dabigatran. It is a potential impurity that may be present in pharmaceutical formulations of Dabigatran, and its presence needs to be monitored and controlled to ensure the safety and efficacy of the drug. Dabigatran iMpurity E is a compound with a specific chemical structure and properties, and its determination and quantification are important for quality control and assurance in the manufacturing process of Dabigatran. It is closely monitored and regulated by pharmaceutical authorities to ensure the safety and effectiveness of the drug for patients.
Used in Pharmaceutical Industry:
Dabigatran iMpurity E is used as a quality control parameter for ensuring the safety and efficacy of Dabigatran, an anticoagulant drug. Its presence in pharmaceutical formulations needs to be monitored and controlled to maintain the drug's effectiveness and to protect patients from potential adverse effects.

1456889-80-7

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  • ethyl 3-(1,2-dimethyl-N-(pyridin-2-yl)-1H-benzo[d]imidazole-5-carboxamido)propanoate

    Cas No: 1456889-80-7

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1456889-80-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1456889-80-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,6,8,8 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1456889-80:
(9*1)+(8*4)+(7*5)+(6*6)+(5*8)+(4*8)+(3*9)+(2*8)+(1*0)=227
227 % 10 = 7
So 1456889-80-7 is a valid CAS Registry Number.

1456889-80-7Relevant articles and documents

SYNTHESIS OF DABIGATRAN

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Page/Page column 41, (2014/10/29)

The present invention relates to a process for preparation of Dabigatran etexilate or pharmaceutically acceptable salt thereof. The present invention relates to novel compounds, in particular Ethyl-3-{[(2-formyl-l-methyl-lH-benzimidazole-5-yl) carbonyl] -(2-pyridinyl) amino} propanoate and Ethyl-3-{[(2-dichloromethyl-l-methyl -lH-benzimidazole-5-yl)carbonyl]- (2-pyridinyl) amino}propanoate and process for preparation thereof. The present invention further relates to the use of these novel compounds in the preparation of Dabigatran etexilate or pharmaceutically acceptable salt thereof.

Synthesis, characterization and suppression of impurities during optimization of dabigatran etexilate

Chen, Yu,Liang, Jun,Chen, Huansheng,Yuan, Li

, p. 1699 - 1710 (2013/09/12)

The synthetic methods for two impurities of dabigatran etexilate are firstly described, and both of two impurities are characterized by NMR and MS spectral data. The suppression of impurities as well as the optimization process of dabigatran etexilate is also disclosed.

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