2-Bromo-6-(trifluoromethyl)pyridine
- CAS No.189278-27-1
- GradeIndustrial / Pharmaceutical
- Availability● In Stock
High-purity 2-Bromo-6-(trifluoromethyl)pyridine designed for advanced organic synthesis and pharmaceutical intermediates.
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Product Overview
2-Bromo-6-(trifluoromethyl)pyridine is a highly specialized fluorinated heterocyclic compound serving as a critical building block in modern medicinal chemistry and agrochemical development. Characterized by the presence of both a bromine substituent and a trifluoromethyl group on the pyridine ring, this molecule offers unique reactivity profiles that are essential for constructing complex molecular architectures. Our manufacturing process ensures exceptional batch-to-batch consistency, making it a reliable choice for research laboratories and large-scale production facilities alike.
The incorporation of the trifluoromethyl moiety is particularly valued in drug design due to its ability to enhance metabolic stability, lipophilicity, and bioavailability of the final active pharmaceutical ingredients. As a trusted global manufacturer, we prioritize purity and safety in every drum shipped.
Technical Specifications
We adhere to strict quality control protocols to guarantee that every shipment meets or exceeds the specified assay requirements. The physical properties listed below are verified through advanced analytical techniques including GC-MS and NMR spectroscopy. Customers can request a Certificate of Analysis (COA) with every order to verify compliance with their internal standards.
| Parameter | Specification |
|---|---|
| CAS Number | 189278-27-1 |
| Molecular Formula | C6H3BrF3N |
| Molecular Weight | 225.99 g/mol |
| Appearance | White crystalline solid |
| Assay | ≥99.0% |
| Melting Point | 48-52°C |
| Boiling Point | 78-79°C |
| Density | 1.707 g/cm3 |
| Refractive Index | 1.471 |
Applications in Pharmaceutical Synthesis
This compound is primarily utilized as a versatile intermediate in organic synthesis. The bromine atom at the 2-position facilitates various cross-coupling reactions, such as Suzuki-Miyaura, Buchwald-Hartwig, and Stille couplings, enabling chemists to introduce diverse functional groups efficiently. Meanwhile, the trifluoromethyl group at the 6-position acts as a powerful electron-withdrawing group, influencing the electronic properties of the pyridine ring and enhancing the binding affinity of downstream drug candidates.
Common applications include the synthesis of kinase inhibitors, GPCR modulators, and other small molecule therapeutics targeting neurological and oncological pathways. Its stability under standard storage conditions makes it suitable for long-term inventory management in chemical warehouses.
Quality Assurance and Storage
To maintain optimal quality, 2-Bromo-6-(trifluoromethyl)pyridine should be stored in a cool, ventilated area away from direct sunlight and moisture. We recommend keeping the container tightly sealed when not in use to prevent degradation. Our packaging options include 25 kg drums, with custom packaging available upon request to suit specific logistical needs. We are committed to providing safe handling guidelines and MSDS documentation to ensure compliance with international safety regulations.
