2,6-二氯碘苯
2,6-二氯碘苯结构式
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常用名 | 2,6-二氯碘苯 | 英文名 | 1,3-Dichloro-2-iodobenzene |
|---|---|---|---|---|
| CAS号 | 19230-28-5 | 分子量 | 272.898 | |
| 密度 | 2.0±0.1 g/cm3 | 沸点 | 268.3±20.0 °C at 760 mmHg | |
| 分子式 | C6H3Cl2I | 熔点 | 64-67 °C(lit.) | |
| MSDS | 中文版 美版 | 闪点 | 116.1±21.8 °C | |
| 符号 |
GHS07 |
信号词 | Warning |
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The comparative metabolism of 2,6-dichlorothiobenzamide (Prefix) and 2,6-dichlorobenzonitrile in the dog and rat.
Biochem. J. 98(3) , 770-81, (1966) 1. A single oral dose of either [(14)C]Prefix or 2,6-dichlorobenzo[(14)C]nitrile to rats is almost entirely eliminated in 4 days: 84.8-100.5% of (14)C from [(14)C]Prefix is excreted, 67.3-79.7% in the urine, and 85.8-97.2% of (14)C from 2,6-dichlorobenzo-[(14... |
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Encapsulation of the uranyl dication. Beer S, et al.
Chem. Sci. 1(1) , 43-47, (2010)
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Non-interconvertible conformers of cupped oxacyclophanes. Grewal RS and Hart H.
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Synthesis of cuppedophanes and cappedophanes. Two new classes of cyclophanes with molecular cavities. Vinod T and Hart H.
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Oxacyclophanes based on a m-terphenyl framework. Grewal RS, et al.
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Zirconium complexes incorporating diaryldiamidoferrocene ligands: generation of cationic derivatives and polymerization activity towards ethylene and 1-hexene. Shafir A and Arnold J.
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