1. Product Overview & Specifications

Key Differentiators: Optimized fluorine substitution enhances reactivity in nucleophilic aromatic substitutions while maintaining thermal stability.

2. Key Applications

Core Use Cases:

• Pharmaceutical Intermediates: Synthesis of fluorinated active pharmaceutical ingredients (APIs)
• Agrochemicals: Building block for herbicides and fungicides
• Liquid Crystal Materials: Fluorine-containing components for electronic displays
• Cross-Coupling Reactions: Suzuki-Miyaura and Buchwald-Hartwig reactions

Performance Advantages:

• Enables precise regioselective modifications
• Enhances compound lipophilicity (LogP optimization)
• Improves metabolic stability in drug candidates

3. Usage Scenarios

Typical Process Integration:

1. Handling: Use inert atmosphere (N₂/Ar) due to moisture sensitivity
2. Reaction Solvents: Compatible with THF, DMF, and dichloromethane
3. Temperature Range: Optimal performance at 0-80°C
4. Catalyst Systems: Effective with Pd(0)/Pd(II) catalysts

Safety Protocols:

• Storage: 2-8°C under inert gas
• PPE Requirements: Chemical-resistant gloves + face protection
• Emergency Measures: Neutralize spills with vermiculite/sand

4. Industry Case Studies

Case 1: Antiviral Drug Intermediate

Client: Top 10 Global Pharma Company
Application: Synthesis of fluorinated nucleoside analog
Result: 22% yield improvement vs. tribromopyridine route

Case 2: Herbicide Formulation

Client: EU Agrochem Producer
Application: Pyridine ring functionalization
Result: Achieved 99.7% regioselectivity at scale

Case 3: OLED Material Development

Client: Asian Electronics Manufacturer
Application: Electron-transport layer component
Result: 15% efficiency gain in prototype devices

5. Contact for Technical Consultation

Request custom synthesis protocols or bulk pricing:
Email: info@vivalr.com
Tel: (86) 15866781826

Service Commitments:
– 24h response time for technical queries
– Batch-specific analytical reports
– Regulatory documentation support