Finerenone

Product Description

Product name: Finerenone
Alias: Finerenone (BAY94-8862); (4S)-4-(4-cyano-2-methoxyphenyl)-5-ethoxy-2,8-dimethyl-1,4-dihydro-1,6-naphthyridine-3-carboxamide; (4S)-4-(4-cyano-2-methoxyphenyl)-5-ethoxy-2,8-dimethyl-1,4-dihydro-1,6-naphthyridine-3-carboxamide; BAY94-8862; BAY948862; 1,6-Naphthyridine-3-carboxamide BAY94-8862;BAY948862;1,6-Naphthyridine-3-carboxamide,4-(4-cChemicalbookyano-2-methoxyphenyl)-5-ethoxy-1,4-dihydro-2,8-dimethyl-,( 4S)-;Finerone;MrNeriketone; (S)-4-(4-Cyano-2-methoxyphenyl)-5-ethoxy-2,8-dimethyl-1,4-dihydro-1,6-naphthyridine-3-carboxamide
CAS No.: 1050477-31-0

Molecular Formula: C21H22N4O3

Molecular weight: 378.42

Properties: white or off-white to yellow powder

Boiling point: 554.7±50.0°C(Predicted)

Density: 1.29±0.1g/cm3(Predicted)

Storage condition: -20°C

*Patented product for research and register use only

Shandong Chenghui Shuangda Pharmaceutical

  • CN
  • 2023
    On CPHI since
  • 3
    Certificates
  • 500 - 999
    Employees
Company types
CMO/CDMO
Manufacturer/Innovator
Pharmaceutical company
Veterinary Company
Primary activities
Animal Health
API Producer
Specifications
  • CAS Registry Number
    1050477-31-0
  • Details
    Assay:No less than 99.0%

  • Selling Points
    Price; Quality Service
  • Supplied from
    China

Shandong Chenghui Shuangda Pharmaceutical

  • CN
  • 2023
    On CPHI since
  • 3
    Certificates
  • 500 - 999
    Employees
Company types
CMO/CDMO
Manufacturer/Innovator
Pharmaceutical company
Veterinary Company
Primary activities
Animal Health
API Producer

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Shandong Chenghui Shuangda Pharmaceutical resources (2)

  • Brochure About us

    Established in 2014, Shandong Chenghui Shuangda Pharmaceutical Co., Ltd. is a leading Chinese manufacturer of active pharmaceutical ingredients (APIs) and advanced intermediates. The company operates 6 cGMP-compliant workshops and 9 automated production lines, delivering a monthly production capacity of 100 metric tons. To date, it has filed 22 products with the Center for Drug Evaluation (CDE) in China, registered 4 APIs in the United States Drug Master File (US-DMF), and submitted 7 applications for Certificates of Suitability (CEP) with the European Directorate for the Quality of Medicines (EDQM)‌.Supported by over 100 patents encompassing advanced synthesis and crystallization technologies‌, the company specializes in API manufacturing and offers integrated CDMO (Contract Development and Manufacturing Organization) and CRO (Contract Research Organization) collaborations.

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    The main production and R & D varieties of local anesthesia, antiviral drugs, cardiovascular and cerebral vascular system, antitumor drugs, digestive drugs, diabetes, veterinary drugs, CDMO products.

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