9-Ethyl-9H-carbazole-3,6-dicarboxaldehyde Cas 70207-46-4

9-Ethyl-9H-carbazole-3,6-dicarboxaldehyde (CAS 70207-46-4) is a carbazole derivative featuring two aldehyde groups at the 3- and 6-positions and an ethyl substitution at the 9-position of the carbazole ring. While specific data for this compound is limited in available literature, its structural analogs and related carbazole derivatives provide insights into its potential properties and applications.

Key Structural Features

• Molecular Formula: Likely C₁₇H₁₄N₂O₂ (estimated based on analogs).
• Molecular Weight: ~278.3 g/mol (approximated).
• Substitutions: 9-ethyl group and aldehyde groups at 3- and 6-positions.

Potential Applications

1. Organic Synthesis: The aldehyde groups make it a versatile intermediate for synthesizing heterocyclic compounds, ligands, or polymers.
2. Pharmaceuticals: Carbazole derivatives are known for antimicrobial, antitumor, and anti-inflammatory activities.
3. Materials Science: Possible use in OLEDs, dyes, or conductive polymers due to carbazole’s electron-rich aromatic system.

Safety Considerations

While specific safety data for this compound is unavailable, related carbazole derivatives (e.g., brominated analogs) exhibit:

• Acute oral toxicity (Category 4)
• Skin and eye irritation potential
• Aquatic toxicity concerns

Recommended precautions include using PPE (gloves, goggles) and ensuring proper ventilation during handling.

Research & Development

For advanced applications, consider:

1. Condensation reactions with amines or hydrazines
2. Coordination chemistry for metal-organic frameworks (MOFs)
3. Polymerization studies for optoelectronic materials

Commercial Inquiry

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Note: This information is based on structural analogs and general carbazole chemistry. Actual properties may vary. Experimental validation is recommended for critical applications.