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About This Item
Linear Formula:
IC6H4OCH2CO2H
CAS Number:
Molecular Weight:
278.04
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
95%
mp
154-157 °C (lit.)
SMILES string
OC(=O)COc1ccc(I)cc1
InChI
1S/C8H7IO3/c9-6-1-3-7(4-2-6)12-5-8(10)11/h1-4H,5H2,(H,10,11)
InChI key
RKORKXFKXYYHAQ-UHFFFAOYSA-N
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Catalytic hypervalent iodine oxidation using 4-iodophenoxyacetic acid and Oxone: oxidation of p-alkoxyphenols to p-benzoquinones.
Yakura T, et al.
Chemical & Pharmaceutical Bulletin, 57(3), 252-256 (2009)
Prediction of acidity constant for substituted acetic acids in water using artificial neural networks.
Habibi-Yangjeh A and Danandeh-Jenagharad M.
Indian J. Chem. B, 46(3), 478-478 (2007)
Chayanis Sutcharitchan et al.
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A simple, rapid, and effective method based on salting-out extraction and LC-MS/MS techniques was developed for the determination of 39 plant growth regulator (PGR) residues in two of the most common root and rhizome Chinese herbs, Codonopsis Radix (Dangshen) and
Muhammet Uyanik et al.
Molecules (Basel, Switzerland), 17(7), 8604-8616 (2012-07-20)
We have developed the first example of hypervalent iodine(V)-catalyzed regioselective oxidation of phenols to o-quinones. Various phenols could be oxidized to the corresponding o-quinones in good to excellent yields using catalytic amounts of sodium salts of 2-iodobenzenesulfonic acids (pre-IBSes) and
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