77 
was obtained from the foregoing by means of methylsulphate at 40° C. 
It melts at 70° C., and erystallizes from ligroin in beautiful, pale 
yellow, transparent crystals. 
Fig. 2. o-Methoxy-m-methyl-benzylidene-aniline. 
Monoclinic-prismatic. 
abs = 12792 0121 0509: 
B 76 IFE 
Forms observed: c= {001}, large and lustrous ; m= {110}, yielding 
good reflexes, like g = {011} also; 7 = 101}, small, but well deter- 
minable. The aspect of the crystals is tabular parallel {O01}. 
Angular values: Observed: Calculated: 
erg = (O01); (OL AI AD — 
em = (O01)-(110) —*~ St 54 — 
m:m = (410) : (410) =* 102 31 = 
c:r =(001):(101)= 44 22 4427 
No distinct cleavage was found. 
The specifie weight of the erystals at 16° C. was: 1,166; the 
molecular volume is therefore: 192,96, and the topical parameters 
are: %: pw: w = 6,7561 : 5,2813 : 5.5502. The form-analogy with the 
red modification of the foregoing substance is undeniable. 
§ 4. III. o-Oxy-m-methyl-«-anilido-ethylbenzene. 
This compound, which melts at 90° C., was obtained from the 
first by means of two molecules of methylmagnesium-iodide in 
boiling etheric solution, and subsequent decomposition of the product 
with water. It has the formula: 
CH, 
en 
< 
OH 
