Compounds > 4-bromophenol

Page last updated: 2024-08-18

4-bromophenol and 4-iodophenol

4-bromophenol has been researched along with 4-iodophenol in 7 studies

Research

Studies (7)

Timeframe	Studies, this research(%)	All Research%
pre-1990	2 (28.57)	18.7374
1990's	0 (0.00)	18.2507
2000's	3 (42.86)	29.6817
2010's	2 (28.57)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Fujita, T; Nakajima, M; Nishioka, T	1
Brent, DA; Frenz, JH; Minick, DJ; Patrick, MA	1
Kapur, S; Rosario, M; Selassie, CD; Verma, RP	1
Abellán Guillén, A; Cordeiro, MN; Garrido Escudero, A; Morales Helguera, A; Pérez-Garrido, A	1
Brooks, SJ; Doyle, EM; Duetz, W; Hewage, C; Malthouse, JP; O' Connor, KE	1
Ashfold, MN; Harvey, JN; King, GA; Murdock, D; Oliver, TA; Sage, AG	1
Chen, G; Du, P; Jin, F; Jin, M; Shao, H; She, Y; Wang, J; Wang, S; Yang, L; Zhang, C; Zheng, L	1

Other Studies

7 other study(ies) available for 4-bromophenol and 4-iodophenol

Article	Year
Hydrogen-bonding parameter and its significance in quantitative structure--activity studies. Journal of medicinal chemistry, 1977, Volume: 20, Issue:8 Topics: Acetylcholinesterase; Anesthetics; Benzene Derivatives; Benzenesulfonates; Carbamates; Chemical Phenomena; Chemistry; Chemistry, Physical; Hydrogen Bonding; Models, Biological; Models, Chemical; Phenoxyacetates; Solubility; Structure-Activity Relationship	1977
A comprehensive method for determining hydrophobicity constants by reversed-phase high-performance liquid chromatography. Journal of medicinal chemistry, 1988, Volume: 31, Issue:10 Topics: Chemical Phenomena; Chemistry, Physical; Chromatography, High Pressure Liquid; Hydrogen Bonding; Mathematics	1988
Cellular apoptosis and cytotoxicity of phenolic compounds: a quantitative structure-activity relationship study. Journal of medicinal chemistry, 2005, Nov-17, Volume: 48, Issue:23 Topics: Animals; Antineoplastic Agents; Apoptosis; Caspases; Cell Line, Tumor; Drug Resistance, Neoplasm; Drug Screening Assays, Antitumor; Enzyme Activation; Mice; Molecular Conformation; Phenols; Quantitative Structure-Activity Relationship; Vinblastine	2005
Convenient QSAR model for predicting the complexation of structurally diverse compounds with beta-cyclodextrins. Bioorganic & medicinal chemistry, 2009, Jan-15, Volume: 17, Issue:2 Topics: beta-Cyclodextrins; Hydrophobic and Hydrophilic Interactions; Organic Chemicals; Quantitative Structure-Activity Relationship	2009
Biotransformation of halophenols using crude cell extracts of Pseudomonas putida F6. Applied microbiology and biotechnology, 2004, Volume: 64, Issue:4 Topics: Biotransformation; Catechols; Chlorophenols; Coenzymes; Iodobenzenes; Phenols; Pseudomonas putida; Substrate Specificity	2004
UV photolysis of 4-iodo-, 4-bromo-, and 4-chlorophenol: competition between C-Y (Y = halogen) and O-H bond fission. The Journal of chemical physics, 2013, Apr-28, Volume: 138, Issue:16 Topics: Chlorophenols; Iodobenzenes; Phenols; Photolysis; Quantum Theory; Ultraviolet Rays	2013
Study on Enhancement Principle and Stabilization for the Luminol-H2O2-HRP Chemiluminescence System. PloS one, 2015, Volume: 10, Issue:7 Topics: Acetone; Acetonitriles; Biphenyl Compounds; Buffers; Dimethylformamide; Horseradish Peroxidase; Hydrogen Peroxide; Hydrogen-Ion Concentration; Imidazoles; Iodobenzenes; Kinetics; Luminescence; Luminescent Measurements; Luminol; Methanol; Organic Chemicals; Phenols; Piperidines; Solvents	2015