| Weight | 232.02 g/mol |
|---|---|
| Formula | C7H5IO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
2-iodobenzaldehyde (26260-02-6)
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- One-pot construction of aza- or oxa-bridged benzocycloheptanes from readily available 2,3-allenyl malonates or 2,3-allenols and o-iodobenzaldehyde or imine. (Organic Letters, 2011)
- Cyclocondensation of 2-iodobenzaldehyde with benzamidines catalyzed by copper(I) iodide: a route to 2-arylquinazolines (Chemistry of Heterocyclic Compounds, 2011)
- Hydrogen-bonded chains of rings in 3-iodobenzaldehyde 2,4-dinitrophenylhydrazone and 4-iodobenzaldehyde 2,4-dinitrophenylhydrazone, and a three-dimensional framework in 4-iodobenzaldehyde 4-nitrophenylhydrazone generated by the combination of N-H...O and C-H...O hydrogen bonds with iodo-nitro interactions. (Acta Crystallographica Section C-crystal Structure Communications, 2004)
- A chain of edge-fused rings generated by the combination of an N-H...O hydrogen bond and an iodo-nitro interaction in 2-iodobenzaldehyde 4-nitrophenylhydrazone versus disordered and effectively isolated molecules in 2-iodobenzaldehyde 2,4-dinitrophenylhydrazone. (Acta Crystallographica Section C-crystal Structure Communications, 2003)
- Synthesis of Indanones via Intramolecular Heck Reaction of Baylis-Hillman Adducts of 2-Iodobenzaldehyde (ChemInform, 2004)
- SYNTHESIS OF 2,4-DIMETHYL-5-IODOBENZALDEHYDE (Organic Preparations and Procedures International, 2002)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C(=C1)C=O)I
-
InChIKeyWWKKTHALZAYYAI-UHFFFAOYSA-N
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