| Weight | 219.025 g/mol |
|---|---|
| Formula | C6H6IN |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2-IODOANILINE (615-43-0)
2-iodobenzenamine
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- Synthesis of 2-Aminobenzothiazole via Copper(I)-Catalyzed Tandem Reaction of 2-Iodobenzenamine with Isothiocyanate (ACS Combinatorial Science, 2009)
- Copper-Catalyzed Double CS Bonds Formation via Different Paths: Synthesis of Benzothiazoles from N-Benzyl-2-iodoaniline and Potassium Sulfide (Organic Letters, 2014)
- Trialkylmanganate-Induced Cyclization of Allyl 2-Iodophenyl Ether, N,N-Diallyl-2-iodoaniline, and alpha-Iodo Acetal. (Journal of Organic Chemistry, 1997)
- Synthesis of 2-aminobenzothiazole via FeCl3-catalyzed tandem reaction of 2-iodoaniline with isothiocyanate in water (Green Chemistry, 2010)
- Electrodeposition of polyaniline, poly(2-iodoaniline), and poly(aniline-co-2-iodoaniline) on steel surfaces and corrosion protection of steel (Applied Surface Science, 2005)
- Palladium-catalysed carbonylation of 4-substituted 2-iodoaniline derivatives: carbonylative cyclisation and aminocarbonylation (Tetrahedron, 2006)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 2-iodobenzenamine
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SMILESC1=CC=C(C(=C1)N)I
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InChIKeyUBPDKIDWEADHPP-UHFFFAOYSA-N
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2-IODOANILINE
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