Alcohols. 



472 



1230 



ALCOHOL C, HmO. 



Phenylbutanediol (HO.CB CMePL 

 Franke, M., 34, (1907 



;alcohol|CkH_ )2 2 



Oxypropylphenyldiethylcarbinol 



HO.CHEt.C 6 H v CEt 2 OH 



<>-. in-, ami p-isomerides. 



Simonis u. Remmert. B., 47, (2307). 



PHENOLS C„H 2 „- 8 2 



PHENOL C 9 H 10 02 



Methyl ether HO.C 6 H 3 (OMe).C 3 H 5 



Eugenol. 



Weinland u. Neff. L15978. Verbin- 

 bundungen des Eugenols mit Eiseu. 



( lompound 

 [Fe{0.C e H s (0Me I ! ,II 6 } jNa 1 aq 



Weinland u. Hermann. 115978. 



PHENOL C2nH 32 02 



Tetradecenylpyrocatechol 



(H()) 2 C 6 H 3 .CH : CH.C 12 H 25 



Dimethyl ether (MeO) 2 C 6 H 3 .C 14 H 27 



Tetradecenylveratrole. 

 Majima & Nakamura 113102. 



PHENOLS CnH 2 „_ 12 2 

 PHENOL C 10 H 8 O 2 



l •• 6-Dioxynaphthalene C 10 H 6 (OH) 3 

 Fischer u. Konig. 110898. Einwir- 

 kung von Phthalsaure-anhydrid aul 1.6- 

 Dioxy-naphtbalin. Bildung von 6.6'- 

 Dioxy-naphthofluoran. 



1 : 4-Dioxynaphthalene. 



4 : 1 TfflODIOXYNAPHTHALENE 



C 10 H 6 (OH)(SB 



Naphtltolmercaptan. 



Ruppersberg. 114688. 1-Naphtol- 

 4-merkaptan. 



PHENOL C 13 H 14 



--Oxy-3-naphthyl-isopropyl alcohol 

 ELO.Ci„H 6 .CMe 2 .OE- 

 Lammer. M., 35, (172). 



PHENOL C 15 H 13 2 



l Oxy-2-naphthyl-diethyl-carbinol 

 HO.C 10 H 8 .CEt 2 .OH 



Preissecker. M., 35, (889). 



PHENOL C.H,.- X4 0i 

 PHENOL CHkO 

 mm-Dioxydibenzyl. 



I lIMETHTL ETHER ( ! 14 H] OW 



Spath. M., 34, (1998). 



ALCOHOLS C..H 2n -i 4 02 

 ALCOHOL C,cH 22 2 



Di-p-tolyl-butanediol 

 C 7 H 7 .CH(OH).CH 2 .CH 2 .CH(OH).C 7 H, 



Dupont. C.R., 158. (714). 



ALCOHOLS C„H.„,- 1S 2 



alcohol C, H 

 Di-p-tolyl-butinenediol 

 C 7 H 7 .CH(OH).C iC.CH OH).C,B 

 Dupont. C.R.,158, (7 1 lj. 



PHENOLS CnH 21 .- 26 2 

 PHENOL C 22 Hi,-0 2 



2 : 2'-Dimethyl-4 : 4'dinaphthol 

 HO.C 10 H 5 Me.C 10 H 5 Me.OE 



Lesser. A., 402, (45). 



PHENOLS C„H 2 „- 28 2 

 PHENOL C23H18O2 



--0xy-3-naphthyldiphenylcarbinol 



HO.C 10 H 8 .CPh 2 .OH 

 and the corresponding Oxynaphthyldi- 

 benzylcarbinol. 

 Lammer. M., 35, (177 



PHENOLS CuH 2 „ - 4 n0 2 

 PHENOL C31H22O2 



2-0xy-3 naphthyl-di-a-naphthyl- 

 carbinol HO.C 10 H 6 .C(C 10 H 7 ) 2 .OH 



Lammer. M., 35, (184). 



TRIOLS. 

 PHENOLS C„H 2 n- 6 3 

 PHENOLS C e H 6 3 



Pyrogallol C 6 H 3 (OH) 3 [l : 2 : 3] 



Bach. 109226. Purpurogallin-Aus- 

 beuten l>ei der Oxydation des Pyro- 

 gallols uiittels Peroxydase and Hydro- 

 peroxyd. 



Weinland u. Denzel. ~ 115976. Eine 

 Pyrogallol-Eisen-Vt'ildiidiiug. 



