Chemical Compound Review:
AGN-PC-0D7DEL 2-ethanoylbenzaldehyde
Synonyms:
CHEMBL394412, AG-E-71798, ACMC-20ao5z, CTK1A2468, KB-227268, ...
Welcome! If you are familiar with the subject of this article, you can contribute to this open access knowledge base by deleting incorrect information, restructuring or completely rewriting any text.
Read more.
Welcome to WikiGenes!
If you are familiar with the subject of this article, you can contribute to this open access knowledge base by deleting incorrect information, restructuring or completely rewriting any text.Ideally this entry shall become one comprehensive and continuous article. Bulleted lists, for instance, were only used because it is impossible to automatically integrate independent facts into a continuous text.
Much of the current information on this page has been automatically compiled from Pubmed.
This precompiled information serves as a substrate and matrix to embed your contributions, but it is by no means the final word - Homo sapiens can do much better!
WikiGenes is a non-profit and open access community project - Read more.
High impact information on ortho-Acetylbenzaldehyde
- We have investigated the photolysis and OH radical reactions of phthaldialdehyde, 2-acetylbenzaldehyde, and 1,2diacetylbenzene, atmospheric reaction products of naphthalene and alkylnaphthalenes, and of phthalide, a photolysis product of phthaldialdehyde [1].
- 8. Blacklamp irradiation showed that phthaldialdehyde and 2-acetylbenzaldehyde photolyze, and, combined with absorption spectra measured in n-hexane solution, average photolysis quantum yields of 0.19 and 0.21, respectively, were derived (290-400 nm) [1].
- The major atmospheric loss process of phthaldialdehyde and 2-acetylbenzaldehyde are estimated to be by photolysis, with photolysis lifetimes of 1.4-1.5 h for a 12-hr average NO2 photolysis rate of 0.312 min(-1) [1].
- Phthalic anhydride was the major observed product from the OH radical-initiated reactions of all four compounds and was also formed from photolysis of phthaldialdehyde and 2-acetylbenzaldehyde [1].
References
- Kinetics and products of photolysis and reaction with OH radicals of a series of aromatic carbonyl compounds. Wang, L., Arey, J., Atkinson, R. Environ. Sci. Technol. (2006) [Pubmed]
Contributions to this collaborative article are from individual authors of WikiGenes or mined by the WikiGenes Data Mining Engine from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.About WikiGenesOpen Access LicencePrivacy PolicyTerms of Useapsburg









