All Photos(1)
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
Recommended Products
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
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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.
Food chemistry, 322, 126766-126766 (2020-04-20)
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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