iodophenol
iodophenol structure
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Common Name | iodophenol | ||
|---|---|---|---|---|
| CAS Number | 533-58-4 | Molecular Weight | 220.008 | |
| Density | 2.0±0.1 g/cm3 | Boiling Point | 187.2±13.0 °C at 760 mmHg | |
| Molecular Formula | C6H5IO | Melting Point | 37-40 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 67.0±19.8 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Regioselective synthesis of 1,3,5-substituted benzenes via the InCl(3)/2-iodophenol-catalyzed cyclotrimerization of alkynes.
J. Org. Chem. 76(20) , 8472-6, (2011) A novel indium(III)-catalyzed cyclotrimerization of alkynes in the presence of 2-iodophenol gave 1,3,5-substituted benzenes in excellent yields with complete regioselectivity. The reaction condition is tolerant to air, and atom economical, in accordance with ... |
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Study on Enhancement Principle and Stabilization for the Luminol-H2O2-HRP Chemiluminescence System.
PLoS ONE 10 , e0131193, (2015) A luminol-H2O2-HRP chemiluminescence system with high relative luminescent intensity (RLU) and long stabilization time was investigated. First, the comparative study on the enhancement effect of ten compounds as enhancers to the luminol-H2O2-HRP chemiluminesc... |
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Highly efficient copper-catalyzed domino ring opening and Goldberg coupling cyclization for the synthesis of 3,4-dihydro-2H-1,4-benzoxazines.
Org. Lett. 11(9) , 1923-6, (2009) trans-3,4-Dihydro-2H-1,4-benzoxazine moieties can be synthesized by domino aziridine ring opening with o-iodophenols followed by the copper-catalyzed Goldberg coupling cyclization (intramolecular C(aryl)-N(amide) bond formation) with good to excellent yields. |
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Copper-catalyzed decarboxylative cross-coupling of alkynyl carboxylic acids with aryl halides.
Chem. Commun. (Camb.) 46(47) , 9049-51, (2010) The copper-catalyzed decarboxylative reactions of alkynyl carboxylic acids with aryl halides were performed under relatively mild reaction conditions. Benzofurans could be further prepared smoothly by a one-pot domino protocol on the basis of decarboxylative ... |
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Fast speciation analysis of iodophenol compounds in river waters by capillary electrophoresis-inductively coupled plasma-mass spectrometry with off-line solid-phase microextraction.
Electrophoresis 25(12) , 1843-51, (2004) An analytical methodology for the fast separation and determination of iodophenol species in natural water samples was developed using capillary electrophoresis (CE) coupled to inductively coupled plasma-mass spectrometry (ICP-MS). Based on the element-specif... |
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Identification of a medicinal off-flavour in mineral water.
Water Res. 43(20) , 5216-24, (2009) The aim of the present study was to identify the compounds responsible for a characteristic medicinal off-odour in mineral water. 2-Dimensional high resolution gas chromatography-mass spectrometry analysis, in combination with olfactometry (HRGC-MS/O), led to... |
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Human liver thermostable phenol sulfotransferase: photoaffinity labeling with 2-iodo-4-azidophenol.
Mol. Pharmacol. 36(6) , 856-65, (1989) Phenol sulfotransferase (PST) catalyzes the sulfate conjugation of phenolic drugs, neurotransmitters, and xenobiotic compounds. Human tissues contain at least two forms of PST, which differ in their substrate specificities, inhibitor sensitivities, physical p... |
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Enhanced competitive chemiluminescent enzyme immunoassay for the trace detection of insecticide triazophos.
J. Food Sci. 77(5) , T99-T104, (2012) A direct competitive chemiluminescent enzyme immunoassay (CLEIA) for triazophos was developed, which was based on the anti-THHe IgG monoclonal antibody and a heterogeneous enzyme tracer (THHu-HRP). Several components of chemiluminescent enhanced solution (CES... |
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Intermediate and mechanism of hydroxylation of o-iodophenol by salicylate hydroxylase.
J. Biochem. 109(5) , 791-7, (1991) Salicylate hydroxylase [EC 1.14.13.1] from Pseudomonas putida catalyzes the hydroxylation of salicylate, and also o-aminophenol, o-nitrophenol, and o-halogenophenols, to catechol. The reactions with these o-substituted phenols comprise oxygenative deamination... |
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Removal of 2-fluoro and 2-iodophenol from aqueous solutions using industrial wastes.
Environ. Technol. 25(1) , 15-22, (2004) A comparative study of the adsorbents prepared from several industrial wastes for the removal of 2-fluorophenol and 2-iodophenol has been carried out. The results show that maximum adsorption on carbonaceous adsorbent prepared from fertilizer industry waste h... |