1,3-Dichloro-2-iodobenzene
1,3-Dichloro-2-iodobenzene structure
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Common Name | 1,3-Dichloro-2-iodobenzene | ||
|---|---|---|---|---|
| CAS Number | 19230-28-5 | Molecular Weight | 272.898 | |
| Density | 2.0±0.1 g/cm3 | Boiling Point | 268.3±20.0 °C at 760 mmHg | |
| Molecular Formula | C6H3Cl2I | Melting Point | 64-67 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 116.1±21.8 °C | |
| Symbol |
GHS07 |
Signal Word | 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.
Tetrahedron Lett. 31(30) , 4271-4274, (1990)
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Synthesis of cuppedophanes and cappedophanes. Two new classes of cyclophanes with molecular cavities. Vinod T and Hart H.
J. Org. Chem. 55(3) , 881-890, (1990)
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Oxacyclophanes based on a m-terphenyl framework. Grewal RS, et al.
J. Org. Chem. 57(9) , 2721-2726, (1992)
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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.
Inorganica Chim. Acta 345 , 216-220, (2003)
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