| Weight | 266.465 g/mol |
|---|---|
| Formula | C7H4ClIO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
2-Iodobenzoyl chloride (609-67-6)
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- Synthesis of isoindolin-1-ones via palladium-catalyzed intermolecular coupling and heteroannulation between 2-iodobenzoyl chloride and imines (Tetrahedron Letters, 2000)
- Synthesis of 3-alkenylisoindolin-1-ones via palladium(0)-catalyzed coupling and cyclization between 2-iodobenzoyl chloride and aldimines (Journal of Heterocyclic Chemistry, 1998)
- SYNTHESIS OF SPIROISOINDOLINONES BY PALLADIUM-CATALYZED HETEROCYCLIZATION OF 2-IODOBENZOYL CHLORIDE WITH KETIMINES (Journal of Heterocyclic Chemistry, 1999)
- ChemInform Abstract: Synthesis of Spiroisoindolinones by Palladium-Catalyzed Heterocyclization of 2-Iodobenzoyl Chloride with Ketimines. (ChemInform, 2010)
- ChemInform Abstract: Synthesis of Isoindolin-1-ones via Palladium-Catalyzed Intermolecular Coupling and Heteroannulation Between 2-Iodobenzoyl Chloride and Imines. (ChemInform, 2010)
- ChemInform Abstract: Synthesis of 3Alkenylisoindolin1ones via Palladium(0)Catalyzed Coupling and Cyclization Between 2Iodobenzoyl Chloride and Aldimines. (ChemInform, 2010)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESC1=CC=C(C(=C1)C(=O)Cl)I
-
InChIKeyMVIVDSWUOGNODP-UHFFFAOYSA-N
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