I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.
2-Iodoaniline is used as an intermediate in organic synthesis.
Gozen Bereket; Evrim Hur; Yucel Sahin. Electrodeposition of polyaniline, poly(2-iodoaniline), and poly(aniline-co-2-iodoaniline) on steel surfaces and corrosion protection of steel. Applied Surface Science. 2005, 252, (5),1233-1244
Qiuping Ding; Banpeng Cao; Xianjin Liu; Zhenzhen Zongand; Yi-Yuan Peng. Synthesis of 2-aminobenzothiazole via FeCl3-catalyzed tandem reaction of 2-iodoaniline with isothiocyanate in water. Green Chemistry. 2010, (9),1607-1610
Quinolines may be synthesized by Pd-catalyzed reaction with allyl alcohols: Tetrahedron Lett., 32, 569 (1991).
Reacts with unsymmetrical acetylenes in the presence of Palladium(II) acetate, 10516, to give indoles substituted at the 2- and/or 3-positions: J. Am. Chem. Soc., 113, 6689 (1991):
Under similar conditions, ketones with an ɑ-methylene group also give indole derivatives: J. Org. Chem., 62, 2676 (1997).
Gefahrenhinweise (EU): H301-H311-H332-H315-H319-H335
Toxic if swallowed. Toxic in contact with skin. Harmful if inhaled. Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.
Avoid breathing dust/fume/gas/mist/vapours/spray. Wear protective gloves/protective clothing/eye protection/face protection. IF SWALLOWED: IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.