This section is from the book "The Volatile Oils Vol1", by E. Gildemeister. Also available from Amazon: The Volatile Oils.

When boiled with alcoholic potassa, safrol is changed to isosafrol.
1) Observations made in the laboratory of Schimmel & Co.
2) Recueil des trav. chim. des P.-B. 4 (1885), 32; Berl. Berichte 23 (1890), 862.
3) Henrard, Chem. Weekblad 4 (1907), 630; Chem. Zentralbl. 1907, II. 1512.
For this compound, which possibly occurs in ylang-ylang oil, the following constants have been determined: d15o 1,124 to 1,129; nD20o1,580.l) B. p. 253 to 254°; dl5o 1,126.2)
With an excess of bromine, isosafrol yields a pentabromide, m. p. 196,5 to 197o.3) Oxidized with chromic acid, it yields piperonal (heliotropin).
In commercial isosafrol, Hoering and Baum4) have demonstrated the presence of two geometric isomers, which they designated a- and B-zsosafrol and of which the latter predominates by far. They are distinguishable only by their odor and their physical constants. Those of a-isosafrol lie between those of safrol and B-isosafrol. Chemically no difference could be observed between the two Isocompounds.
 
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