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Chemical Compound Review

o-Jodfenol     2-iodophenol

Synonyms: o-Jodphenol, o-Iodophenol, PubChem3963, SureCN5720, CHEMBL225564, ...
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High impact information on o-Jodphenol

  • On the other hand, the intramolecular cyclization of the prenyl ether of 2-iodophenol would proceed in a fashion similar to the conventional palladium-catalyzed transformation [1].
  • Inhibitors of the reaction catalyzed by TS PST, including 2,6-dichloro-4-nitrophenol-3'-phosphoadenosine- 5'-phosphate and NaCl, as well as 2-iodophenol, a competing substrate, inhibited the photolabeling of both of these proteins by [125I]IAP in a concentration-dependent fashion [2].
  • Intermediate and mechanism of hydroxylation of o-iodophenol by salicylate hydroxylase [3].

Biological context of o-Jodphenol


Associations of o-Jodphenol with other chemical compounds


  1. Cobalt-catalyzed trimethylsilylmethylmagnesium-promoted radical alkenylation of alkyl halides: A complement to the Heck reaction. Affo, W., Ohmiya, H., Fujioka, T., Ikeda, Y., Nakamura, T., Yorimitsu, H., Oshima, K., Imamura, Y., Mizuta, T., Miyoshi, K. J. Am. Chem. Soc. (2006) [Pubmed]
  2. Human liver thermostable phenol sulfotransferase: photoaffinity labeling with 2-iodo-4-azidophenol. Otterness, D.M., Powers, S.P., Miller, L.J., Weinshilboum, R.M. Mol. Pharmacol. (1989) [Pubmed]
  3. Intermediate and mechanism of hydroxylation of o-iodophenol by salicylate hydroxylase. Suzuki, K., Gomi, T., Itagaki, E. J. Biochem. (1991) [Pubmed]
  4. Hydroxylation of o-halogenophenol and o-nitrophenol by salicylate hydroxylase. Suzuki, K., Gomi, T., Kaidoh, T., Itagaki, E. J. Biochem. (1991) [Pubmed]
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