4-Chloro-2-iodoaniline
4-Chloro-2-iodoaniline structure
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Common Name | 4-Chloro-2-iodoaniline | ||
|---|---|---|---|---|
| CAS Number | 63069-48-7 | Molecular Weight | 253.468 | |
| Density | 2.0±0.1 g/cm3 | Boiling Point | 295.0±25.0 °C at 760 mmHg | |
| Molecular Formula | C6H5ClIN | Melting Point | 40 °C | |
| MSDS | Chinese USA | Flash Point | 132.2±23.2 °C | |
| Symbol |
GHS05, GHS06 |
Signal Word | Danger | |
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Quinazolines. VI. Synthesis of 2,4-diaminoquinazolines from anthranilonitriles.
J. Med. Chem. 13(5) , 882-6, (1970)
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A tandem Heck-carbocyclization/Suzuki-coupling approach to the stereoselective syntheses of asymmetric 3,3-(diarylmethylene)indolinones.
J. Org. Chem. 70(9) , 3741-4, (2005) [reaction: see text] An efficient and versatile method for stereoselective synthesis of (E)-3,3-(diarylmethylene)indolinones by a palladium-catalyzed tandem Heck-carbocyclization/Suzuki-coupling sequence is presented. Factors influencing yield and selectivity... |
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Stereoselective Synthesis of (E)-3-(Methoxycarbonyl) methylene-1, 3-dihydroindol-2-ones by Palladium-Catalyzed Oxidative Carbonylation of 2-Ethynylanilines. Gabriele B, et al.
European J. Org. Chem. 24 , 4607-4613, (2001)
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Regioselective iodination of aryl amines using 1, 4-dibenzyl-1, 4-diazoniabicyclo [2.2. 2] octane dichloroiodate in solution and under solvent-free conditions. Alikarami M, et al.
Bull. Chem. Soc. Ethiop. 29(1) , 157-162, (2015)
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