| Weight | 134.178 g/mol |
|---|---|
| Formula | C9H10O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
4-Methoxystyrene (637-69-4)
4-vinylanisole
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- Visible Light Photoinitiated Metal-Free Living Cationic Polymerization of 4-Methoxystyrene (Journal of the American Chemical Society, 2015)
- Acid Generation Mechanism of Poly(4-hydroxystyrene)-Based Chemically Amplified Resists for Post-Optical Lithography: Acid Yield and Deprotonation Behavior of Poly(4-hydroxystyrene) and Poly(4-methoxystyrene) (Japanese Journal of Applied Physics, 2006)
- Synthesis of Branched Polystyrene and Poly(styrene-b-4-methoxystyrene) by Nitroxyl Stable Radical Controlled Polymerization (Macromolecules, 2001)
- Nanosecond and Picosecond Dynamics of the Radical Cation Mediated Dimerization of 4-Methoxystyrene (Journal of the American Chemical Society, 1994)
- Melting behavior, miscibility, and hydrogen-bonded interactions of poly(-caprolactone)/poly(4-hydroxystyrene-co-methoxystyrene) blends (Journal of Polymer Science Part B, 1998)
- Copolymerization kinetics of 4-methoxystyrene with methyl methacrylate and 4-methoxystyrene with styrene: A test of the penultimate model (Journal of Polymer Science Part A, 1990)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 4-vinylanisole
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SMILESCOC1=CC=C(C=C1)C=C
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InChIKeyUAJRSHJHFRVGMG-UHFFFAOYSA-N
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Similar Compounds
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4-Methoxystyrene
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