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5-(2-Fluorophenyl)-1H-Pyrrole-3-Carboxaldehyde
This high-purity intermediate is a critical component in the synthesis of Vonoprazan Fumarate, a leading potassium-competitive acid blocker designed to treat various acid-related gastrointestinal conditions. Its precise chemical structure and quality ensure the efficacy and safety of the final Active Pharmaceutical Ingredient (API).
- Facilitating the synthesis of the novel acid blocker Vonoprazan Fumarate, crucial for treating gastrointestinal issues.
- As a key component in API manufacturing, this intermediate ensures product integrity and efficacy.
- The high purity of this pharmaceutical intermediate meets stringent industry standards for R&D and production.
- Enabling advancements in drug discovery, this building block supports the development of new treatments for acid-related diseases.
Advantages Offered
Reliable Pharmaceutical Synthesis
Utilizing this intermediate ensures a reliable pathway for Vonoprazan Fumarate Intermediate synthesis, minimizing batch-to-batch variability in API production.
Enhanced Drug Efficacy
The superior quality of the 5-(2-Fluorophenyl)-1H-Pyrrole-3-Carboxaldehyde pharmaceutical grade intermediate contributes directly to the enhanced therapeutic efficacy of the final drug product.
Streamlined R&D Processes
With guaranteed purity and adherence to specifications, this CAS 881674-56-2 bulk drug intermediate streamlines research and development efforts in creating effective treatments.
Key Applications
API Manufacturing
Essential for the large-scale production of Vonoprazan Fumarate, this intermediate is vital for API manufacturers aiming for quality and compliance.
Drug Discovery
Supports pioneering research in developing new therapies for acid-related disorders, leveraging its specific chemical properties.
Custom Synthesis Projects
Serves as a foundational compound for custom synthesis projects requiring specialized pharmaceutical building blocks.
Quality Control and Analysis
Used as a reference standard for analytical reagents and quality control in the pharmaceutical industry.