Unlock the Synthesis of Gemcitabine with a Key Intermediate
Discover the essential chemical compound that drives the production of vital anticancer therapies.
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2-Deoxy-2,2-difluoro-D-erythro-pentofuranose-3,5-dibenzoate-1-methanesulfonate
This advanced chemical intermediate is pivotal for the synthesis of Gemcitabine hydrochloride, a cornerstone medication in cancer treatment. Its precise chemical structure and high purity are critical for ensuring the efficacy and safety of the final pharmaceutical product. We focus on delivering this vital component to support pharmaceutical research and development.
- Gemcitabine intermediate synthesis relies on this compound for efficient and reliable production pathways.
- As a crucial chemical intermediate for anticancer drugs, its quality directly impacts therapeutic outcomes.
- Sourcing this high-purity precursor ensures consistency in complex pharmaceutical manufacturing processes.
- The compound's unique chemical properties make it an indispensable building block in advanced organic synthesis.
Advantages You Gain
Reliable Supply Chain
Ensure uninterrupted production of your pharmaceutical products by securing a dependable cas 122111-11-9 supplier with consistent quality.
Exceptional Purity
Benefit from a high purity gemcitabine precursor, crucial for meeting stringent pharmaceutical quality standards and regulatory requirements.
Expert Technical Support
Leverage our expertise in pharmaceutical intermediate sourcing to navigate complex chemical procurement and ensure optimal product performance.
Key Applications
Anticancer Drug Synthesis
This compound serves as a fundamental building block in the multi-step process for creating potent anticancer agents like Gemcitabine.
Pharmaceutical Research & Development
Essential for laboratories engaged in developing new cancer therapies and optimizing existing drug synthesis routes.
Fine Chemical Manufacturing
A specialized chemical used in sophisticated organic synthesis processes where precise molecular structures are paramount.
Quality Control Standards
Can be utilized as a reference standard in quality control processes to verify the identity and purity of related pharmaceutical compounds.
Related Technical Articles & Resources
Why Choose Us?
Leverage our expertise and state-of-the-art infrastructure to accelerate your journey from discovery to commercial success.
Global Experience
With 20 years of R&D, manufacturing, and sales experience, we proudly serve clients across 60 countries and regions worldwide.
Advanced Facilities
Our in-house R&D laboratory, pilot platform, and large-scale production workshop are equipped to meet the audit requirements of global customers.
Seamless Scalability
We facilitate a perfect transition from small-scale lab requirements (grams) to full commercialization (hundreds of tons).