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Thermo Scientific Chemicals
4-Methoxystyrene, 98%, stab. with 0.1% 4-tert-butylcatechol
CAS: 637-69-4 | C9H10O | 134.18 g/mol
化学物質識別子
CAS637-69-4
仕様
スペックシート
スペックシートAssay (GC)≥97.5%
Appearance (Color)Clear colorless to yellow
Identification (FTIR)Conforms
FormLiquid
Refractive Index1.5585-1.5635 @ 20°C
4-Methoxystyrene is employed in the ferric chloride-catalyzed addition of activated methylenes to styrenes. It acts as a monomer in polymerization reactions. Further, it is used to prepare 1,1,2,2-Tetracyano-3-(p-methoxyphenyl)cyclobutane by reacting with ethenetetracarbonitrile.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
4-Methoxystyrene is employed in the ferric chloride-catalyzed addition of activated methylenes to styrenes. It acts as a monomer in polymerization reactions. Further, it is used to prepare 1,1,2,2-Tetracyano-3-(p-methoxyphenyl)cyclobutane by reacting with ethenetetracarbonitrile.
Solubility
Slightly miscible with methanol.
Notes
Light sensitive. Store in cool place. Incompatible with strong oxidizing agents and strong acids.
4-Methoxystyrene is employed in the ferric chloride-catalyzed addition of activated methylenes to styrenes. It acts as a monomer in polymerization reactions. Further, it is used to prepare 1,1,2,2-Tetracyano-3-(p-methoxyphenyl)cyclobutane by reacting with ethenetetracarbonitrile.
Solubility
Slightly miscible with methanol.
Notes
Light sensitive. Store in cool place. Incompatible with strong oxidizing agents and strong acids.
RUO – Research Use Only
General References:
- Perkowski, A. J.; You, W.; Nicewicz, D. A. Visible Light Photoinitiated Metal-Free Living Cationic Polymerization of 4-Methoxystyrene. J. Am. Chem. Soc. 2015, 137 (24), 7580-7583.
- Miyazawa, K.; Koike, T.; Akita, M. Regiospecific Intermolecular Aminohydroxylation of Olefins by Photoredox Catalysis. Chem. Eur. J. 2015, 21 (33), 11677-11680.