Alcohols. 



558 



1230 



Hextl ether. 



6-Cliloroliexyl plienyl etlier 



a.(CHj)6.0Ph 



and C)-iodoliexijl phenyl ether. 



Braun, J. von und Miiller, C. Berlin, 

 Ber. D. cliem. Ges., 39, 1906, (4110- 

 4119). 



DlPHENTL SULPHIDE (CjH5)2S 



also the o-sitPvO- and o-amino- 



DEEIVATIVES. 



Mauthner, F. t.e. (3593-3598). 



O- and p- OXYDIPHEXYL SULPHIDE CjjHioOS 



Methyl ether C,3HijOS 



Mauthner, F. I.e. 



nun- and pp- DioxYWPHEyTL sulphide 



S(C6H,.0H), 



Dimethyl ether. 



Mauthner, F. I.e. 



DiPHESTL DISELEXIDE. 



Stoecker, M. und KrafFt, F. Oxydation 

 Ton Diphenyldiselenid, (06115)2882. i.e. 

 (2197-2201). 



Chlorophexols. 

 Giese, W. Einwirkung vonChlor auf 

 den p-Oxybenzaldehyd. Tetra- und 

 Pentachlori^henol u. Derivate. Diss. 

 Kiel, 1905. 



Brouophenols. 

 - : 3 : 5-Tribroviophenol. 



Bamberger, E. und Kraus, E. Berlin, 

 Ber. D. cliem. Ges., 39, 1906, (4248- 

 4252). 



NiTROPHESOLS. 



aci-2 : 4-DixiTROPHESOL. 



Ethyl ether. 



Hantzsch, A. und Gorke, H. t.e. 

 (1073-1084). 



aci-TEIS ITROPHEXOL. 



Ethyl ether (^02)2 C6H2<^^q q-^^ 



and the methyl ether. 



Hantzsch, A. und Gorke, H. I.e. 



2:4: 6-Trisitropuenol 



• (Picric acid). 



Bruni, G. e Tomani, E. Sui picrati 

 di composti non saturi. [isometileuge- 

 uolo, isosafrolo, isoapiolo, asarone.] 

 (h\7.7.. chim. ital., Roma, 34,11, 1904, 

 (474-479). Rist. da Roma, Rend. Ace. 

 Lincei, fSer. 5), 13, ii, 1904, (184-187). 



Levin, M. Theorie der Loslichkeits- 

 beeinfiussung. [Pikriusaure.] Diss. 

 Gottingen, l'J04 ; Zs. phvsik. Chem., 

 Leipzig, 55, 1906, (513-536). 



Orlov, E. I. Condensation des oxy- 

 acides et du formaldehyde sous Faction 

 de I'acide picrique. (Russ.) St. Peter- 

 burg, Zurn. russ. lis. -chim. ObSc., 38, 

 1906, (1211-1216). 



Methyl ether. 



Sudborough, J. J. and Picton, N. 



[Additive compound of methyl picrate 

 ■with ethvl-a-naphthvlamine.j London, 

 J. Chem.Soc, 89, 1906, (583-595). 



Amixophexols v. 1630. 



PHENOLS CtHsO 



Cresols CeH.Me.OH 

 Bauer, H. Desinfektionskraft der 

 Kresole. Siidd. ApothZtg, Stuttgart, 

 46, 1906, (513). 



o-Cresol. 

 Kortenbach, J. Chlorierungspro- 

 dukte des o-Kresols und ihr Verhalten 

 gegen Brom imd Salpetersaure. Diss. 

 Marburg, 1905. 



Zineke, Th. und Hedenstrom, A. 

 Einwirkung von Brom auf o-Kresol. 

 Liebigs Ann Chem., Leipzig, 350, 1906, 



(269-287). 



00-, oni-, and ?nm-DiTOLTL sulphide 



Mauthner, F. Berlin, Ber. D. chem. 

 Ges., 39, 1906, (3593-3598). 



Bromo-o-cresols. 



Mono-, di-, tri- and tetra-hromo- 



derivatives. 



3 : 5-Xitrohromo-, 3, 4, 5-nitrodihromo- 



and 3:4:5: 6-nitrotrihromo-com pounds 



and the pseudo-bromides. 



Zineke, Th. und Hedenstrom, A. 

 Liebigs Ann. Chem., Leipzig, 350, 1906, 

 (269-287). 



Dibromo-o-oxybenzyl bromide. 



Piperidine, methylamine, benzylamine 



and diamylamirie derivatives. 



Auwers, K. und Schroeter, O. op. 

 cit. 344, 1906, (141-170;. 



Tetrabromo-o-oxybenzyl bromide. 



Piperidine, methylamine, benzylamine 



and diamylamine compounds. 



Auwers, K. und Schroeter, 0. I.e. 



