2-Fluoro-5-Nitro-6-Picoline: Technical Guide & Industry Applications
Table of Contents
- 1. Product Specifications & Comparative Analysis
- 2. Key Applications in Pharmaceutical & Chemical Industries
- 3. Operational Protocols & Handling Guidelines
- 4. Industry Use Cases
- 5. Client Success Stories
- 6. Request Customized Solutions
1. Product Specifications & Comparative Analysis
| Parameter | 2-Fluoro-5-Nitro-6-Picoline | 2-Chloro-5-Nitro-6-Picoline | 5-Nitro-6-Picoline (Unsubstituted) |
|---|---|---|---|
| CAS Number | 1268524-17-7 | N/A | 5335-04-4 |
| Molecular Formula | C6H4FN3O2 | C6H4ClN3O2 | C6H6N2O2 |
| Molecular Weight | 169.11 g/mol | 185.57 g/mol | 138.12 g/mol |
| Fluorine Content | 11.23% | 0% | 0% |
| Thermal Stability | Stable up to 250°C | Decomposes at 200°C | Stable up to 280°C |
2. Key Applications in Pharmaceutical & Chemical Industries
Pharmaceutical Intermediates: Critical building block for kinase inhibitors and antiviral agents. The fluorine atom enhances metabolic stability in API development.
Agrochemical Synthesis: Used in next-generation neonicotinoid derivatives with improved pest selectivity.
Coordination Chemistry: Serves as ligand precursor for transition metal catalysts in cross-coupling reactions.
3. Operational Protocols & Handling Guidelines
Storage: Maintain under inert gas (Ar/N2) at 2-8°C in amber glass containers
Reaction Compatibility: Compatible with Pd-catalyzed couplings (Suzuki, Buchwald-Hartwig) at 0.5-2 mol% loading
Safety: PPE Requirements: Nitrile gloves, chemical goggles, and Type 4B respirator for powder handling
4. Industry Use Cases
Case A: Oncology Drug Development – Used in third-stage synthesis of FGFR inhibitors (85% yield improvement vs. chloro analogs)
Case B: Crop Protection Agents – Key intermediate in systemic insecticides with 40% reduced environmental persistence
5. Client Success Stories
ABC Pharma (Germany): Reduced lead compound synthesis steps from 7 to 4 using our GMP-grade material in PKCθ inhibitor development.
AgroChem Solutions (USA): Achieved EPA approval 5 months faster for novel aphicide using our custom fluorinated picoline derivatives.
University Research Lab (Japan): Published Nature Chemistry paper on asymmetric catalysis using our specialty material as chiral directing group.
6. Request Customized Solutions
Our technical team provides:
- Custom synthesis from mg to kg scale
- Regulatory support for FDA/EMA submissions
- Stability testing & impurity profiling
Contact our specialists:
Email: info@vivalr.com
Tel: (86) 15866781826


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