| Weight | 424.143 g/mol |
|---|---|
| Formula | C13H13IO8 |
| Hydrogen Acceptors | 8 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
Dess-Martin periodinane (87413-09-0)
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- A useful 12-I-5 triacetoxyperiodinane (the Dess-Martin periodinane) for the selective oxidation of primary or secondary alcohols and a variety of related 12-I-5 species (Journal of the American Chemical Society, 1991)
- An improved procedure for the preparation of the Dess-Martin periodinane (Journal of Organic Chemistry, 1993)
- A Useful 12-I-5 Triacetoxyperiodinane (the Dess-Martin Periodinane) for the Selective Oxidation of Primary or Secondary Alcohols and a Variety of Related 12-I-5 Species. (ChemInform, 1991)
- Iodine(V) reagents in organic synthesis. Part 1. Synthesis of polycyclic heterocycles via Dess-Martin periodinane-mediated cascade cyclization: generality, scope, and mechanism of the reaction. (Journal of the American Chemical Society, 2002)
- Iodine(V) reagents in organic synthesis. Part 2. Access to complex molecular architectures via Dess-Martin periodinane-generated o-imidoquinones. (Journal of the American Chemical Society, 2002)
- Synthesis of Imides, NAcyl Vinylogous Carbamates and Ureas, and Nitriles by Oxidation of Amides and Amines with DessMartin Periodinane (Angewandte Chemie, 2005)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(=O)OI1(C2=CC=CC=C2C(=O)O1)(OC(=O)C)OC(=O)C
-
InChIKeyNKLCNNUWBJBICK-UHFFFAOYSA-N
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