2-Methoxy-6-vinylnaphthalene (CAS number 63444-51-9), supplied by TCI as product M3588, is an aromatic vinyl monomer belonging to the group of small-molecule building blocks for organic semiconductors. This compound plays an important role in the materials laboratory as a raw material for the synthesis of conjugated polymers and naphthalene derivatives used in organic electronics research. The conjugated naphthalene core, combined with a reactive vinyl group, makes this compound a key component for controlled polymerization and copolymerization reactions. In the laboratory, it is used to develop active materials for devices such as organic light-emitting diodes (OLEDs), organic solar cells, and organic field-effect transistors, making it a versatile and widely applicable reagent for advanced materials research.
The main advantage of this compound lies in the combination of methoxy and vinyl substituents on the naphthalene ring. The methoxy group acts as an electron donor that can modulate the energy levels of molecular orbitals, so the optical and electronic properties of the resulting synthesized materials can be adjusted according to research needs. At the same time, the vinyl group provides a reactive site for polymer chain growth, enabling the preparation of conjugated polymers with controlled structure and chain architecture. This dual functionality makes 2-Methoxy-6-vinylnaphthalene a preferred choice for researchers seeking reproducible, tunable building blocks when designing active materials for organic electronic applications, as it offers both chemical versatility and predictable behavior in synthesis.
In Indonesian laboratories, this compound is typically applied to develop active materials for devices such as OLEDs, organic solar cells, and organic field-effect transistors. It is also frequently used as a comparison and reference material in studies of structure–electronics relationships and in spectroscopic characterization work. Materials science groups and chemistry laboratories in Indonesia rely on this TCI-grade building block to support research programs focused on organic semiconductors, conjugated polymer synthesis, and the development of next-generation electronic materials, where consistent quality and reliable batch-to-batch performance are essential for valid experimental results.
- Conjugated polymer synthesis: The reactive vinyl group enables controlled polymerization, making this monomer a dependable starting material for constructing conjugated polymer backbones in organic electronics research and materials development.
- OLED active-layer development: The methoxy electron-donor group tunes molecular orbital energy levels, helping researchers formulate emissive or charge-transport materials for organic light-emitting diode device testing.
- Organic solar cell material research: The extended conjugation of the naphthalene core makes this compound suitable for building donor or acceptor components used in the photoactive layers of organic photovoltaic devices.
- Structure–electronics correlation studies: As a well-defined reference compound, it supports systematic investigations that link molecular structure to optical and electronic behavior during spectroscopic characterization experiments.
- Copolymerization and functionalization experiments: The vinyl functionality allows incorporation into copolymers with other aromatic monomers, enabling tailored band-gap and solubility profiles for device fabrication trials.
| Brand | TCI |
|---|---|
| CAS number | 63444-51-9 |
| Molecular formula | — |
| Purity | — |
| Category | Materials Science > Material Building Blocks > Small Molecule Semiconductor Building Blocks |
| Pack sizes | As supplied by TCI; pack size and physical form should be confirmed on the product label or catalog entry at the time of ordering. |
| Physical form | — |
| Storage | — |
- Product code: M3588
- Product name: 2-Methoxy-6-vinylnaphthalene
Store in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and ignition sources, as the vinyl group makes the compound reactive toward polymerization. Keep the container tightly closed when not in use and protect it from moisture and prolonged exposure to air. Use containers made of materials compatible with organic compounds, such as glass or suitable laboratory-grade plastics, and avoid transferring the material to unlabeled vessels. Wear appropriate personal protective equipment, including gloves and safety glasses, and work in a fume hood. Avoid contact with skin and eyes, and keep the material away from strong oxidizing agents and polymerization initiators. Follow standard laboratory hygiene practices and dispose of any waste according to local regulations.
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