6-Chloro-2-fluoropurine
- CAS No.1651-29-2
- GradeIndustrial / Pharmaceutical
- Availability● In Stock
High-purity 6-Chloro-2-fluoropurine intermediate for pharmaceutical synthesis. Reliable supply with comprehensive quality documentation.
Request Bulk PricingProduct Technical Details
Product Overview
6-Chloro-2-fluoropurine stands as a pivotal heterocyclic compound within the realm of modern medicinal chemistry. As a halogenated purine derivative, this chemical building block plays an essential role in the development of novel therapeutic agents. Our facility specializes in the production of high-grade intermediates that meet stringent international standards for pharmaceutical research and development. This specific purine analogue is characterized by its unique substitution pattern, which offers distinct reactivity profiles suitable for complex organic synthesis pathways.
We understand that consistency and purity are paramount when selecting raw materials for drug discovery. Therefore, our manufacturing processes are designed to minimize impurities and ensure batch-to-batch reproducibility. Whether you are developing anti-viral medications or exploring new oncology treatments, having access to reliable chemical intermediates is the foundation of successful project outcomes.
Chemical Properties and Specifications
The structural integrity of 6-Chloro-2-fluoropurine allows for versatile functionalization during synthesis. The presence of both chloro and fluoro substituents on the purine ring system provides chemists with multiple handles for nucleophilic substitution reactions. Below are the detailed physical and chemical parameters verified through our quality control laboratories.
| Parameter | Specification |
|---|---|
| CAS Number | 1651-29-2 |
| Molecular Formula | C5H2ClFN4 |
| Molecular Weight | 172.55 g/mol |
| Appearance | Off-white to yellow powder |
| Purity (HPLC) | ≥98.0% |
| Melting Point | 162-163°C |
| Density | 1.766 g/cm3 |
| Boiling Point | 553.2°C |
Industrial Applications
This compound is primarily utilized as a key intermediate in the synthesis of nucleoside analogues. These analogues are frequently investigated for their potential in treating various viral infections and malignant tumors. The halogen atoms facilitate coupling reactions necessary for constructing more complex molecular architectures found in active pharmaceutical ingredients. Researchers value this material for its stability under standard storage conditions and its predictable behavior during synthetic transformations.
Furthermore, the high purity level ensures that downstream reactions proceed with minimal side products, thereby simplifying purification processes and improving overall yield. Our clients in the biotechnology and pharmaceutical sectors rely on this material for lead optimization and scale-up activities. It serves as a critical component in the pipeline for developing next-generation therapeutics.
Quality Assurance and Logistics
Quality control is integrated at every stage of our production cycle. Each batch undergoes rigorous testing using high-performance liquid chromatography and other analytical methods to confirm identity and assay values. We provide a comprehensive Certificate of Analysis with every shipment to ensure full transparency and compliance with your internal quality standards.
Packaging is designed to maintain product integrity during transit. Standard options include 25 kg drums, though we offer flexible packaging solutions tailored to specific customer requirements. Storage recommendations include keeping the material in a cool, ventilated area away from direct sunlight and moisture. Our global logistics network ensures timely delivery to support your research and manufacturing schedules without interruption.
