Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Edit custom filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1948 1
1987 1
1995 1
2000 1
2002 2
2003 1
2005 1
2006 1
2007 1
2008 4
2009 2
2010 1
2011 4
2012 1
2013 2
2014 2
2015 1
2016 3
2017 3
2019 4
2020 4
2023 2
2024 1
2025 2
2026 4

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

45 results

Results by year

Filters applied: . Clear all
Quoted phrases not found in phrase index: "2-methylbenzenecarbonal", "o-toluic aldehyde", "o-toluylaldehyde", "o-tolylaldehyde"
Page 1
The atmospheric photolysis of o-tolualdehyde.
Clifford GM, Hadj-Aïssa A, Healy RM, Mellouki A, Muñoz A, Wirtz K, Martín Reviejo M, Borrás E, Wenger JC. Clifford GM, et al. Environ Sci Technol. 2011 Nov 15;45(22):9649-57. doi: 10.1021/es2026533. Epub 2011 Oct 27. Environ Sci Technol. 2011. PMID: 22007606
The photolysis of o-tolualdehyde by natural sunlight has been investigated at the large outdoor European Photoreactor (EUPHORE) in Valencia, Spain. The photolysis rate coefficient was measured directly under different solar flux levels, with values in the range j( …
The photolysis of o-tolualdehyde by natural sunlight has been investigated at the large outdoor European Photoreactor (EUPHORE …
Food Protective Effects of 3-Methylbenzaldehyde Derived from Myosotis arvensis and Its Analogues against Tyrophagus putrescentiae.
Park JH, Lee NH, Yang YC, Lee HS. Park JH, et al. Sci Rep. 2017 Jul 26;7(1):6608. doi: 10.1038/s41598-017-07001-5. Sci Rep. 2017. PMID: 28747743 Free PMC article.
Based on the LD(50) values, 2,4,5-trimethylbenzaldehyde (0.78 mug/cm(3)) had highest vapor action against T. putrescentiae, followed by 2,4-methylbenzaldehyde (1.14 mug/cm(3)), 2,5-dimethylbenzaldehyde (1.29 mug/cm(3)), 2-methylbenzaldehyde (1.32 mug/cm(3)), 2,3-dim …
Based on the LD(50) values, 2,4,5-trimethylbenzaldehyde (0.78 mug/cm(3)) had highest vapor action against T. putrescentiae, followed by 2,4- …
Wavelength Dependence of Light-Induced Cycloadditions.
Menzel JP, Noble BB, Lauer A, Coote ML, Blinco JP, Barner-Kowollik C. Menzel JP, et al. J Am Chem Soc. 2017 Nov 8;139(44):15812-15820. doi: 10.1021/jacs.7b08047. Epub 2017 Oct 25. J Am Chem Soc. 2017. PMID: 29024596
The pi pi* transition of the carbonyl group of the o-methylbenzaldehyde correlates with a highly efficient conversion to the cycloadduct, showing no significant wavelength dependence, while conversion following the n pi* transition proceeds markedly less efficie …
The pi pi* transition of the carbonyl group of the o-methylbenzaldehyde correlates with a highly efficient conversion to the …
Pressure-Dependent Kinetics of o-Xylene Peroxy Radical Chemistry.
Li Y, Zhang X, Xu X. Li Y, et al. J Phys Chem A. 2026 Mar 26;130(12):2621-2632. doi: 10.1021/acs.jpca.6c00250. Epub 2026 Mar 17. J Phys Chem A. 2026. PMID: 41843649
High-precision theoretical calculations were performed to investigate the kinetics of reactions involving o-methylbenzylperoxy radical (RO(2) ) and o-hydroperoxymethyl-benzyl radical ( QOOH), including their formation by the reaction of o-xylyl radical with O(2), as well as the c …
High-precision theoretical calculations were performed to investigate the kinetics of reactions involving o-methylbenzylperoxy radical (RO(2 …
A method of detecting carbonyl compounds in tree leaves in China.
Huang J, Feng Y, Fu J, Sheng G. Huang J, et al. Environ Sci Pollut Res Int. 2010 Jun;17(5):1129-36. doi: 10.1007/s11356-009-0277-3. Epub 2009 Dec 17. Environ Sci Pollut Res Int. 2010. PMID: 20016999
Seven carbonyl compounds, including formaldehyde, acetaldehyde, acetone, acrolein, p-tolualdehyde, m/o-tolualdehyde, and hexaldehyde were determined and quantified. The most common carbonyl species of the four tree leaves were formaldehyde, acrolein, and m/o- …
Seven carbonyl compounds, including formaldehyde, acetaldehyde, acetone, acrolein, p-tolualdehyde, m/o-tolualdehyde, and hexal …
Isolation of a Pseudomonas stutzeri strain that degrades o-xylene.
Baggi G, Barbieri P, Galli E, Tollari S. Baggi G, et al. Appl Environ Microbiol. 1987 Sep;53(9):2129-32. doi: 10.1128/aem.53.9.2129-2132.1987. Appl Environ Microbiol. 1987. PMID: 3674872 Free PMC article.
The organism grew on 2,3- and 3,4-dimethylphenol but not on 2-methylbenzyl alcohol, o-tolualdehyde, or o-toluate. P. stutzeri was not able to utilize m-xylene, p-xylene, or 1,2,4-trimethylbenzene, but growth was observed in the presence of the corresponding alcohols …
The organism grew on 2,3- and 3,4-dimethylphenol but not on 2-methylbenzyl alcohol, o-tolualdehyde, or o-toluate. P. stutzeri …
Mapping Photochemical Reactivity Profiles on Surfaces.
Michalek L, Krappitz T, Mundsinger K, Walden SL, Barner L, Barner-Kowollik C. Michalek L, et al. J Am Chem Soc. 2020 Dec 30;142(52):21651-21655. doi: 10.1021/jacs.0c11485. Epub 2020 Dec 18. J Am Chem Soc. 2020. PMID: 33337866
On surfaces, the relationship between the surface absorption spectra and reactivity remains unexplored. Thus, herein, the reactivity of an o-methylbenzaldehyde and a tetrazole, as ligation partners for maleimide functionalized polymers, was investigated when the rea …
On surfaces, the relationship between the surface absorption spectra and reactivity remains unexplored. Thus, herein, the reactivity of an …
Inhibitory effects on mushroom tyrosinase by some alkylbenzaldehydes.
Chen QX, Song KK, Wang Q, Huang H. Chen QX, et al. J Enzyme Inhib Med Chem. 2003 Dec;18(6):491-6. doi: 10.1080/14756360310001613094. J Enzyme Inhib Med Chem. 2003. PMID: 15008513 Free article.
The results show that the alkylbenzaldehydes assayed can lead to reversible inhibition to the enzyme; o-tolualdehyde and m-tolualdehyde are mixed-type inhibitors and p-alkylbenzaldehydes are uncompetitive inhibitors. ...The inhibitory effects of alkylbenzaldehydes o …
The results show that the alkylbenzaldehydes assayed can lead to reversible inhibition to the enzyme; o-tolualdehyde and m-tol …
Efficient synthesis of benzo(hetero)aryl-5-yl(2-hydroxyphenyl)methanones via mechanochemical benzannulation.
Xu Q, Cui Q, Wang J. Xu Q, et al. Chem Commun (Camb). 2026 Jan 20;62(5):1601-1605. doi: 10.1039/d5cc06020f. Chem Commun (Camb). 2026. PMID: 41427934
Upon sp(3) C-H activation, unprecedented benzannulations of 2-methylbenzaldehyde and 2-methylindole-3-carbaldehyde with 3-formylchromones were successfully achieved, accompanied by significantly reduced E-factors. ...
Upon sp(3) C-H activation, unprecedented benzannulations of 2-methylbenzaldehyde and 2-methylindole-3-carbaldehyde with 3-form …
45 results