4-AMINO-7-(TRIFLUOROMETHYL)QUINOLINE

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4-Amino-7-(Trifluoromethyl)Quinoline Overview

This fluorinated quinoline derivative (CAS 112022-64-9) serves as a premium building block in pharmaceutical and advanced material synthesis. The trifluoromethyl group enhances both metabolic stability and lipophilicity compared to non-fluorinated analogs.

Technical Specifications & Competitive Analysis

Parameter Specification Analog Compound Competitive Advantage
Purity ≥99.5% (HPLC) 98% typical Superior reaction efficiency
Solubility DMSO >50mg/mL ~30mg/mL Better formulation flexibility
Thermal Stability Stable up to 250°C 220°C decomposition Enhanced process safety

Core Application Areas

Pharmaceutical Intermediate

Critical component in:

  • Kinase inhibitor development (EGFR/VEGFR)
  • Antimalarial drug candidates
  • PET tracer precursors

Material Science

  • OLED electron transport layers
  • Coordination polymer synthesis

Implementation Scenarios

Lab-scale Synthesis Protocol

Typical reaction conditions:

Step Conditions Yield
Cyclization DMAc, 120°C, 8h 82-85%
Fluorination CuI catalyst, 80°C 91%

Industrial Production

Batch process optimization parameters:

  • 500L reactor capacity
  • GMP-compliant purification
  • 15kg/batch output

Documented Client Implementations

Case 1: Oncology Research Institute

Challenge: Develop brain-penetrant EGFR inhibitors
Solution: Utilized compound’s CF3 group for blood-brain barrier penetration
Outcome: 3 lead compounds with IC50 < 10nM

Case 2: Electronic Materials Producer

Challenge: Create stable blue OLED emitters
Solution: Incorporated as electron-deficient moiety
Result: 18% EQE improvement vs. baseline

Request Customized Solutions

Available modifications:

  • Isotope-labeled versions (13C/15N)
  • Bulk quantities (100kg+)
  • GMP-grade material

Contact our technical team:
Email: info@vivalr.com
Tel: (86) 15866781826

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