Quality Level
assay
95%
refractive index
n20/D 1.474 (lit.)
bp
58 °C/13 mmHg (lit.)
density
0.87 g/mL at 25 °C (lit.)
SMILES string
CC1C(C)=C(C)C(C)=C1C
InChI
1S/C10H16/c1-6-7(2)9(4)10(5)8(6)3/h6H,1-5H3
InChI key
WQIQNKQYEUMPBM-UHFFFAOYSA-N
General description
研究了顺磁性内层金属富勒烯与 1,2,3,4,5-五甲基环戊二烯的 Diels-Alder 反应机理。报道了 1,2,3,4,5-五甲基环戊二烯的三步法大规模合成。用激光烧蚀质谱法研究了 1,2,3,4,5-五甲基环戊二烯 (HCp*) 在气相中与钯离子的反应。它与富含电子的烯烃发生自由基阳离子催化的环加成反应,生成 Diels-Alder 产物。
Application
1,2,3,4,5-五甲基环戊二烯用作:
- 五羰基铁中的金属有机溶剂蒸汽沉积中的生长调节剂化学品。
- 通过肟的中间体将醇催化转化为酰胺的“一锅法”铱中的配体。
- 合成[Cp*Rh(bpy)H2O]2+(Cp* = 五甲基环戊二烯基,bpy = 2,2′-联吡啶),它是 NADH 再生过程中的电子介质。
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商品
The Diels–Alder reaction is the reaction between a conjugated diene and an alkene (dienophile) to form unsaturated six-membered rings. It is also referred to as a cycloaddition.
An improved synthesis of 1,2,3,4,5-pentamethylcyclopentadiene.
Kohl FX and Jutzi P.
Journal of Organometallic Chemistry, 243(1), 119-121 (1983)
Synth. React. Inorg. Met.-Org. Chem. , 24, 395-395 (1994)
Journal of Organometallic Chemistry, 472, 359-359 (1994)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 214027-5G | 04061838773098 |
| 214027-25G | 04061838773081 |
