Weight | 278.045 g/mol |
---|---|
Formula | C8H7IO3 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 3 |
4-Iodophenoxyacetic acid (1878-94-0)
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- Hypervalent iodine oxidation of phenol derivatives using a catalytic amount of 4-iodophenoxyacetic acid and Oxone as a co-oxidant (Tetrahedron, 2010)
- Catalytic Hypervalent Iodine Oxidation of p-Dialkoxybenzenes to p-Quinones Using 4-Iodophenoxyacetic Acid and Oxone (Chemical & Pharmaceutical Bulletin, 2008)
- Efficient synthesis of p-quinols using catalytic hypervalent iodine oxidation of 4-arylphenols with 4-iodophenoxyacetic acid and oxone. (Chemical & Pharmaceutical Bulletin, 2009)
- Catalytic Hypervalent Iodine Oxidation Using 4-Iodophenoxyacetic Acid and Oxone: Oxidation of p-Alkoxyphenols to p-Benzoquinones (Chemical & Pharmaceutical Bulletin, 2009)
- A Novel Catalytic Hypervalent Iodine Oxidation of p-Alkoxyphenols to p-Quinones Using 4-Iodophenoxyacetic Acid and Oxone. (Synlett, 2007)
- Synthetic plant-growth regulators. I. 2,4-dichloro-5-iodophenoxyacetic acid and derivatives (Journal of Organic Chemistry, 1949)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=CC=C1OCC(=O)O)I
-
InChIKeyRKORKXFKXYYHAQ-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
Similar Compounds
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methyl 2-(4-hydroxyphenoxy)acetate
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