7-CHLORO-4-HYDROXY-2-(TRIFLUOROMETHYL)QUINOLINE

7-Chloro-4-hydroxy-2-(trifluoromethyl)quinoline: Comprehensive Guide for Researchers & Industry Professionals

Table of Contents

• Product Specifications & Comparative Analysis
• Key Applications & Industrial Uses
• Synthesis Protocol & Handling Guidelines
• Industry Case Studies
• Technical Inquiry & Ordering Process

1. Product Specifications & Comparative Analysis

2. Key Applications & Industrial Uses

This specialty quinoline derivative demonstrates exceptional performance in:

• Pharmaceutical intermediates for kinase inhibitors
• Organic light-emitting diode (OLED) materials
• Antimicrobial agent development
• Fluorescent probes for cellular imaging

3. Synthesis Protocol & Handling Guidelines

Step 1: Prepare reaction vessel with anhydrous DMF under nitrogen atmosphere
Step 2: Add 2-trifluoromethylquinolin-4-ol (1.0 equiv) and N-chlorosuccinimide (1.2 equiv)
Step 3: Maintain reaction at 80°C for 6 hours
Safety Note: Use chemical-resistant PPE and conduct reactions in fume hood

4. Industry Case Studies

Case Study 1: Pharmaceutical Development (ABC Therapeutics)

Challenge: Required high-purity intermediate for Phase III clinical trial material
Solution: Custom synthesis with 99.8% purity achieved
Outcome: 40% improvement in reaction yield compared to previous supplier

Case Study 2: Materials Science (NanoLum Technologies)

Challenge: Needed thermally stable electron-transport layer material
Solution: Optimized crystal structure modification
Outcome: Increased OLED device lifetime by 300 hours

5. Technical Inquiry & Ordering Process

For batch-specific COA, custom synthesis requests, or bulk pricing:
Email: info@vivalr.com
Phone: (86) 15866781826

Request quotation template:
1. Required quantity (mg to kg scale)
2. Purity requirements
3. Preferred shipping method
4. Project timeline