1230 513 



Dinitroanmio-p-cresol 

 [1:3:5:2:4] C6HMe(X02)2NHj . OH 



Sommer, A. J. prakt. C'hem., Leip- 

 zig, (X.F.), 67, 1903, (513-573;. 



Din'Uromelhylaminocresol 

 [1:3:5:2:4] C6HMe(N02)2(NHMe) . OH 



Sommer, A. J. prakt. Cheiii., Leip- 

 zig, (X.F.), 67, 1003, (513-573). 



Aminoditolyl sulphide 

 [4 : 1] CeH.Me . S . C^U^Me . NH2 [1:2:4] 



Meyer. E[rnst]. Ueber das p-Thio- 

 tolyl-m-toluidin. J. prakt. Chem., 

 Leipzig, (N.F.), 68, 1903, (289-294). 



Zur Kenntnis der Para- 



Toluolsulfinsaure. 2. Abh. Ueber 

 p-Thiotolylanilia und p-Thiotolyltolui- 

 cline. J. prakt. Chem., Leipzig, (N.F ) 

 68, 1903, (263-2G5). 



Aminoditolyl sulphide 

 [4:1] f'^H^Me . S . CgHjMe . NH^ [1 : 3 : 4] 



Meyer, Ernst. Ueber p-Thiotolyl-o- 

 toluidin. J. prakt. Chem., Leipzio- 

 iX.F.), 68, 1903, (279-289). °' 



PHENOLS CsHioO 



Xylenols CeHjMea.OH 

 Bromo-derivatives. 

 Crossley, Arthur William and Le 

 Sueur, Henry Rondel. [Bromoxylenol 

 (m.p. 83.5-84"). Dibromoxylenol 



(m.p. 96.5^. Two tribromoxylenols 

 (m.p. 176-177.5^ and 182-183 ).] Lon- 

 tlon, J. Chem. Sec, 83, 1903, (12(5-129); 

 [abstract] Proc. Chem. Soc., 18. 190*^ 

 (239). 



Noelting, E. Berichtigimg iiber 

 Broinxylenole. Berlin, Ber. D. chem 

 Ges., 36, 1903, (656). 



BROMO-m-XYLENOL 



CfiHjMejBr . OH [1 : 3 : 5 : 4] 

 Ethers : CeH^MeaBr . . CHj . CH^Br 



and (CelljMe^Br . 0)2C2H4 

 Stoermer, R. und Oohl, Fr. Berlin 

 Ber. D. chem. Ces., 36, 1903, (2873- 

 2877). 



(D-3482) 



1230 



Methyl ether C6H3Me2 . OMe 

 Blanksma, J. J. [La brorauration et 

 la nitration de I'ether methylique du 

 xylenol symetrique.] Rec. Trav. chim., 

 Leiden, 21, 1902, (328-335). 



Aming-xylenol 



C6H2Me2(NH2)(OH) [5:3:4:1] 



Methyl ether C8H2Me2(NH2) . OMe 



(2, 6-D imethyl-1-a minoA-mel hoxy- 

 benzene) 



Bamberger, Eug. Berlin, Ber. D. 

 chem. Ges., 36, 1903, (2028-2041). 



0-, m-, and 2>Ethylphenols. 



Methyl ethers MeO . C6H4Et 



(Ethylanisoles). 



Klages, August. Berlin, Ber. D. 

 chem. Ges., 36, 1903, (3584-3597). 



PHENOLS CsHnO 



1, 3, 5Trimethyl-2-oxybenzene. 



TeIMETHTLOXY-4, 6-Dn.SOCYANOBENZENE. 



Kaufler. F. Wien, MonHfte Chem., 

 22, 1901, (1073-1082). 



PHENOLS C10H14O 



Thymol CJIjMe^CjH,) . OH [5 : 2 : l] 



Dannenberg. Paul. Ueber eiuige 

 Jod und Bromderivate des Thymols. 

 Wien, MonHfte Chrm., 24, 1903 (67- 



79). ^ 



Dekker, G. et Solonina, B. Sur la 



structure des matieres colorantes 

 nitrosees du thymol. (Russe.) St. Peter- 

 burg, Zurn. russ. fiz.-chim. ObSc., 35. 

 1903, (718-742, av. 1 tabl.). 



. — ; Sur la con- 

 stitution des couleurs nitrosees du thymol. 

 (Russe) St. Peterburg. ^urn. russ' fiz.- 

 chim. ObSc., 35, 1903, (936-953, av. 



2 tabl.). 



Hedman, Karl. Ueber das Thymol 

 als Anthebninticum. (Schwedisch) 

 F. Lakares. HandL, Hclsincfors, 1, 1903, 



(23-26). 



