| Weight | 219.025 g/mol |
|---|---|
| Formula | C6H6IN |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
3-IODOANILINE (626-01-7)
o-iodoaniline
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LabBot
- Palladium-catalyzed synthesis of quinolines from allylic alcohols and o-iodoaniline (Tetrahedron Letters, 1991)
- Syntheses and Structures of the Complexes cis-[M(C(6)F(5))(2)(NaX)] (M = Pd, Pt; NaX = 2-Iodoaniline, 2-Benzoylpyridine) Containing NaX Acting as a Didentate Chelating Ligand and Displaying I-->M or O-->M Interactions. (Inorganic Chemistry, 1996)
- Conversion of 2-iodoaniline into (Z)-3-methylene-2,3-dihydroindole derivatives (Heterocycles, 1991)
- REACTION OF O-IODOANILINE WITH AROMATIC KETONES IN DMSO : SYNTHESIS OF 2-ARYL OR 2-HETARYLINDOLES (Synthesis, 1999)
- The Structure of the Cyclodextrin Complex. XI. Crystal Structure of Hexakis(2,3,6-tri-O-methyl)--cyclodextrinp-Iodoaniline Monohydrate (Bulletin of the Chemical Society of Japan, 1982)
- First syntheses of two quinoline alkaloids from the medicinal herb Ruta Chalepensis via cyclization of an o-iodoaniline with an acetylenic sulfoneElectronic supplementary information (ESI) available: experimental data and NMR spectra. See http://www.rsc.org/suppdata/cc/b2/b205408f/ (Chemical Communications, 2002)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - o-iodoaniline
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SMILESC1=CC(=CC(=C1)I)N
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InChIKeyFFCSRWGYGMRBGD-UHFFFAOYSA-N
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