Talk:Phloroglucinol
This article is rated Start-class on Wikipedia's content assessment scale. It is of interest to the following WikiProjects: | |||||||||||||||||||||
|
Layout error
editThe image sequence is ovelapped by the info box. __meco 02:47, 15 July 2006 (UTC)
The second compound in the synthetic pathway is 1,3,5 trinitrobenzene. It is NOT a "nitrate," that would be an alcohol ester of nitric acid with the functional group -NO3; (example PETN). Perhaps this is a common trade name like nitrogylcerin; (which is a nitrate ester)? Also the rainey nickel/hydrogen reductant used in the nitro to the amine reaction is not an explosive. It is just a very (spontaneously) flammable mix. Paul S.
-- added melting point and mol weight. Boris W. I understand that this is a known, deadly carcinogen by old Eastman Kodak. Are scientitsts getting evil by the moment, or do they need to revisit what they are doing? For humanity? I'm a European Anthropologist. Try out Professor Noam Chomsky, if you really want a sober, subside
LV@torgaugin.@sshypocrite
Pictures needed for 1,3,5-cyclohexanetrione
editThe infobox should display also pictures of the tautomer 1,3,5-cyclohexanetrione. --Jorge Stolfi (talk) 06:30, 30 June 2009 (UTC)
Position of equilibrium
editCan we assign %s to the two forms? Can they be isolated at low enough temperature? --Jorge Stolfi (talk) 06:29, 30 June 2009 (UTC)
various problems
editChemistry - the "Many such monophenolics..." sentence does not make sense here (and I suggest deleting "still" in the previous sentence or just deleting this whole paragraph). Typo - figure - UV visible spEctrum. "...but it does sublime" - if it melts it does not sublime. (It might sublime at reduced pressure). Synthesis - there should be a dash between 1,3,5 & trinitrobenzene. Biosynthesis - 3,5-diketoheptanoate product. Phloroglucinol cannot be dehydroxylated to get hydroxyquinol (that would be an isomerization if it occurred). Potential health effects - Phloroglucinols acylated - either delete the s or add '. Applications - change in to by after minimized. Ref. 8 is missing a space. In Chemistry I suggest changing "found along with two isomers," to "one of three isomers along with". 69.72.92.27 (talk) 22:13, 29 November 2015 (UTC)
GHS Labelling Source
editWhere does the GHS pictogram and H/P statements come from? Does not seem to be correct. 2A02:3100:75E2:FC00:C576:8AFF:B1:24E7 (talk) 17:46, 21 May 2024 (UTC)
Citations
edit21 & 23 I think are broken links - they don't link to a .PDF or are broken links. I don't know about others. W;ChangingUsername (talk) 12:05, 3 July 2024 (UTC)
Sources provide another routes of preparing phloroglucinol.
edita description from Italian wikipedia's article about the chemical's tautomers
editLa molecola esiste in due forme tautomere: 1,3,5-triidrossibenzene e 1,3,5-cicloesantrione. I due tautomeri sono in equilibrio secondo la reazione: Ktsquare (talk) 15:35, 15 September 2024 (UTC)