茚
| 茚 | |
|---|---|
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| IUPAC名 1H-indene | |
| 识别 | |
| CAS号 | 95-13-6 |
| PubChem | 7219 |
| ChemSpider | 6949 |
| SMILES |
|
| InChI |
|
| InChIKey | YBYIRNPNPLQARY-UHFFFAOYAJ |
| Beilstein | 635873 |
| Gmelin | 27265 |
| ChEBI | 41921 |
| DrugBank | DB02815 |
| KEGG | C11565 |
| 性质 | |
| 化学式 | C9H8 |
| 116.16 g·mol⁻¹ | |
| 若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。 | |
茚也被称为苯并茂,自然界中存在于煤焦油175-185 °C 馏分中。可以通过钠和茚反应(茚是酸性的),然后水蒸气蒸馏将茚分离出来。
参考资料
- W. v. Miller, Rohde (1889). "Zur Synthese von Indenderivaten". Berichte der deutschen chemischen Gesellschaft 22 (2): 1881 - 1886. doi:10.1002/cber.18890220227.
- W. v. Miller, Rohde (1890). "Zur Synthese von Indenderivaten". Berichte der deutschen chemischen Gesellschaft 23 (2): 1881 - 1886. doi:10.1002/cber.18900230228.
- W. v. Miller, Rohde (1890). "Zur Synthese von Indenderivaten". Berichte der deutschen chemischen Gesellschaft 23 (2): 1887 - 1902. doi:10.1002/cber.18900230227.
- Finar, Il (1985). Organic Chemistry. Longman Scientific & Technical. ISBN 0-582-44257-5.
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