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Cinnamyl alcohol is an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff. It is also used in perfumery and as well as a deodorant.
E Armengol.; ML Cano.; A Corma.; H García. Mesoporous aluminosilicate MCM-41 as a convenient acid catalyst for Friedel-Crafts alkylation of a bulky aromatic compound with cinnamyl alcohol. Journal of the Chemical Society, Chemical Communications.19957 (1), 519-520.
RL Mansell.; GG Gross.; J Stöckigt.; H Franke.; MH Zenk. Purification and properties of cinnamyl alcohol dehydrogenase from higher plants involved in lignin biosynthesis. Phytochemistry. 19747 (1), 519-520.
Protection of carboxylic acids as cinnamyl esters has been reported: J. Chem. Soc., Chem. Commun., 707 (1996). They can be cleaved under neutral conditions with Hg(II) or KSCN: Tetrahedron Lett., 2081 (1977).
Allylic alcohols react with primary or secondary amines in the presence of SnCl2 and a Pd(0) catalyst to give allylic amines regioselectively: Chem. Lett., 1121 (1995):
Gefahrenhinweise (EU): H302-H315-H319-H317
Harmful if swallowed. Causes skin irritation. Causes serious eye irritation. May cause an allergic skin reaction.
Do not get in eyes, on skin, or on clothing. Wear protective gloves/clothing. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.