■juiyr."i??iarm"}    Developments  in  Organic  Compounds. 
,OH 
329 
Betol        C6H  / 
xCOJ  —  C10H7 
OH 
Salacetol  C6H4^ 
xCOO  —  CH0COCH3 
Salophen    C6H  '  NH 
XCOO  •  C6H  / 
XCOCH. 
OH 
Cresalols  QH^ 
Salicylic  nap  thy  I 
ester. 
Salicyl  acetol. 
A  ceto-pa  ra  -  a  mid 0  - 
salol. 
So  lie y lie  ere sy lie 
estets. 
COO  •  C6H4CH3 
As  esters  of  Guaiacol 
OH  (!) 
XOCH3  (2) 
we  have  the  valuable  comparatively  tasteless  and  less  disturbing 
compounds 
O  — C6H4OCH3 
Duotal  CO' 
xO— CeH4OCH3 
,OH 
QH3s 
■OCH3  +  2H20 
Benzosol  C6H4; 
COOH 
OCH.: 
O  —  C6H.CO 
OCR 
Guaiacol  carbonate. 
Guaiacel  carbonic 
acid 
Guaiaeol  benzoate. 
Guaiacol  cinnamate. 
Sty  r  a  col  QH/ 
X0 — C6H4 — CH-— CH — CO 
OCH3 
Geosote      QH/  Guaiacol  valerate. 
xO— COCH,— CH=(CH3)2 
^  ru   /OCH3  Guaiacol  glyceryl 
Guaiamar  CHH/  .       &  s  j 
xO— CH2— CHOH— CH2OH  eUur- 
ANTIPYRETICS. 
Formerly  the  efforts  of  the  synthetic  chemist  were  directed  toward 
producing  bodies  analogous  in  character  and  action  to  the  well  known 
quinin.    Ten  years  ago  the  views  as  to  the  constitution  of  quinin  were 
