Talk:Cinnamic acid

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Untitled[edit]

Does anyone know what the IR of trans-cinnamic Acid looks like? because mine looks very similar to that of Camphor

The article incorrectly refers to the reaction as a Claisen condensation. I changed it to refer to the aldol condensation (with accompanying hydrolysis of the anhydride) Azmanam (talk) 14:49, 7 April 2016 (UTC)[reply]

MALDI-MS[edit]

Its use in MALDI-MS would be great. Aaadddaaammm 01:16, 4 November 2006 (UTC)[reply]

WikiProject Food and drink Tagging[edit]

This article talk page was automatically added with {{WikiProject Food and drink}} banner as it falls under Category:Food or one of its subcategories. If you find this addition an error, Kindly undo the changes and update the inappropriate categories if needed. The bot was instructed to tagg these articles upon consenus from WikiProject Food and drink. You can find the related request for tagging here . Maximum and careful attention was done to avoid any wrongly tagging any categories , but mistakes may happen... If you have concerns , please inform on the project talk page -- TinucherianBot (talk) 01:03, 4 July 2008 (UTC)[reply]

Solubility[edit]

The solubility given for this compound is incomplete. It should be stated what substance it is soluble in, what temperature this occurs at, and the correct units. As it stands, none of these requirements have been met. — Preceding unsigned comment added by Numinin (talk • contribs) 01:14, 8 September 2011 (UTC)[reply]

Add reference to Truxillic acids[edit]

Cinnamon acid is often found with truxillic acids; due to photocatalyzed formation of cyclobityl ring. Shjacks45 (talk) 22:18, 9 May 2019 (UTC)[reply]

Which was first (citation needed tag)[edit]

The Ullman ref states that the Perkins reaction is the oldest one used for commercial production. This is properly sourced and can be stated with confidence in the article until information counter to that surfaces. --Lpd-Lbr (talk) 15:02, 16 September 2019 (UTC)[reply]