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Thermo Scientific Chemicals
1H-Indene, 90+%, stab. with 0.01% 4-tert-butylcatechol
CAS: 95-13-6 | C9H8 | 116.163 g/mol
化学物質識別子
CAS95-13-6
IUPAC Name1H-indene
Molecular FormulaC9H8
InChI KeyYBYIRNPNPLQARY-UHFFFAOYSA-N
SMILESC1C=CC2=CC=CC=C12
さらに表示
仕様
スペックシート
スペックシートAssay (GC)≥90.0%
Appearance (Color)Clear colorless to yellow to brown
CommentMay contain some polymer
Refractive Index1.5660-1.5760 @ 20?C
FormLiquid
1H-Indene is a building block that has been used in the synthesis of isatins. It was used in the synthesis of new C60 derivative, indene-C60 bisadduct. It was used in preparing polyindene by the controlled cationic polymerization initiated with cumyl methyl ether/TiCl4 in CH2Cl2.
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
1H-Indene is a building block that has been used in the synthesis of isatins. It was used in the synthesis of new C60 derivative, indene-C60 bisadduct. It was used in preparing polyindene by the controlled cationic polymerization initiated with cumyl methyl ether/TiCl4 in CH2Cl2.
Solubility
Soluble in ethanol, acetone, ethyl ether, and ether. Insoluble in water.
Notes
Store at 4°C. Store in dark. Incompatible with oxidizing agent, light, heat.
1H-Indene is a building block that has been used in the synthesis of isatins. It was used in the synthesis of new C60 derivative, indene-C60 bisadduct. It was used in preparing polyindene by the controlled cationic polymerization initiated with cumyl methyl ether/TiCl4 in CH2Cl2.
Solubility
Soluble in ethanol, acetone, ethyl ether, and ether. Insoluble in water.
Notes
Store at 4°C. Store in dark. Incompatible with oxidizing agent, light, heat.
RUO – Research Use Only
General References:
- Youjun He; Hsiang-Yu Chen; Jianhui Hou; Yongfang Li.Indene-C(60) bisadduct: a new acceptor for high-performance polymer solar cells. Journal of the American Chemical Society. 2010, 132 (4), 1377-1382.
- Hahn SF and Hillmyer MA. High glass transition temperature polyolefins obtained by the catalytic hydrogenation of polyindene. Macromolecules. 2003, 36 (1), 71-76.