Product Name: 9-Fluorenone
CAS Number: 486-25-9
Description:
9-Fluorenone is a vital aromatic organic compound, appearing as a distinctive bright yellow crystalline solid. Structurally derived from fluorene, it serves as a crucial intermediate and building block in various organic synthesis processes. Its unique chemical structure makes it highly valuable in the development of pharmaceuticals, specialty dyes, and advanced functional materials. We supply high-purity 9-Fluorenone suitable for demanding research, development, and manufacturing applications.
Properties:
| Property | Value |
| Chemical Formula | |
| Molar Mass | |
| CAS Number | 486-25-9 |
| Appearance | Bright yellow crystalline solid |
| Melting Point | 81-85 |
| Boiling Point | 341.5 |
| Solubility | Insoluble in water; Soluble in common organic solvents (e.g., ethanol, ether, benzene, chloroform) |
| Synonyms | Fluoren-9-one, 9H-Fluoren-9-one |
| Purity | >98% |
| Storage Conditions | Store in a cool, dry, well-ventilated area away from incompatible substances. Keep container tightly closed. |
Usage:
9-Fluorenone is a versatile intermediate primarily utilized in organic synthesis. Its applications span several fields:
- Pharmaceutical Synthesis: It acts as a precursor or key intermediate in synthesizing various active pharmaceutical ingredients (APIs).
- Example: Used in the development pathways for certain antimalarial drugs, antihypertensives, and other therapeutic agents.
- Dyes and Pigments: Its chromophoric structure makes it suitable for creating specialty dyes and pigments.
- Example: Incorporated into molecules designed for specific colorimetric properties or sensing applications.
- Functional Materials: It is used in the synthesis of polymers and materials with specific optical or electronic properties.
- Example: Employed in creating materials for organic light-emitting diodes (OLEDs) or photovoltaic applications.
- Chemical Research: Serves as a standard reagent and building block in academic and industrial research laboratories for developing new molecules and reactions.