Amines. 



CSS 



1630 



solution dans racide siilfuiique. (Russ.) 

 St Peterburg, Zurn. riiss. fis.-chini. 

 Obsc., 38, 19015, (959-962). 



Wieland, H. und Gamtoarjan, S. Die 

 Oxvdation des Diiihenvhimiiis. Berlin, 

 Bei-. D. cheuj. Ges., 39, 1906, (1499- 

 1506). 



TRISlTRODirnEUTLAMIXE 



C6H,(N02)3.NHPli 



Sudborough, J. J. and Picton, N. 



[Additive coniponnd of picrj'laniline 

 •uith a-naplithvlanjine.] London, J. 

 Chem. Sec, 89,' 1906, (583-595). 



HEXANITRODIPHEXVLAillNE. 



Mulder, A. Preparation de quelques 

 liexanitrodiphenj-lamines [substituees]. 

 Rec. Trav. chim., Leiden, 25, 1900, 

 (121-123). 



Diphenylmethylamine 



{Methyldiphenylamine) 

 23, p'-DiBKOMO and o, o', j-), p'-teteabkomo- 



il ETHYLDirilEN YLAMKE. 



Also tlie Perhroviide 

 (C6H4Br)2NMe.HBr.Br2 



Fries, K. Liebigs Ann. Chem., 

 346, 1906, (128-219). 



AMINES C;HgN 



Toluidine CII3.C6II4 :NH2 



Slijper, H. J [Vergleichende] kri- 

 stallograpliische (jntersnchung der 

 isomeren Acet- und Benztoluide. (Holltin- 

 disch) Groniugen, 1906, (5-1). 



o-Toluidine. 



Reuter, 0. Einwirkuug von Phosgen 

 auf Diniethyl-o-Toluidin und ilono- 

 aethyl-o-Toluidin in Gegenwart von 

 Aluminiumchlorid. Diss. Leipzig, 1904. 



Phosphoric acid derivatives 



(C7H7NH)4P.OEt, (C,H,NH)4PC1 



and (C7H,NH)4P.N03 



Lemoult, P. Paris, Bui. soc. chim., 

 (ser. 3), 35, 1906, (-17-66). 

 o-Toluidine phosphite CHjNHz.HjPOj 

 Lemoult, P. Paris, C.-R. Acad, sci., 

 142, 190U, (1193-1195). 



DlTHIOMAI.ONYL DERIVATIVE 



C17H13N2S2 i-e. 

 C7H,.NH.CS.CH2.CS.NH.C7H7 

 also the p-isomeride. 

 Reissert, A. und Mor^, A. Berlin, D. 

 clieni. Ges., 39, 1906, (3298-3308). 



4-NlTRO-O-TOLLIDlXE. 



Morgan, G. T. and Micklethwait, 

 F. ]\I. G. [with Couzens, E. O.] Benzene- 

 sulphonyl-4-nitro-o-toluidine 



"xC^.C'eHaMe.XH.SOjPh 

 and its reduction. London, J. Chem. 

 Soc, 89, 1906, (1289-1300). 



wi-Toluidine 



2>I0DU-7?1-T0LU1I)1KE 



Willgerodt, C. und Simonis, M. Ber- 

 lin, Ber. D. chem. Ges., 39, 1906, (269- 

 280). 



p-Toluidine. 



Liljeblad, F. Umlagerungsprodukte 

 von Methylen-di-p-Tolyliniid. Diss., 

 Leipzig. 19*05. 



Additive compoimd with trinitrotoluene 

 C6H2Me(N02)3,C6H,Me.NH2 



Jackson, C. L. and Clarke, L. London, 

 Proc. Cliem. Soc, 22, 1906, (83-84). 



Methyl-o- toluidine 



5-Bro-\io and 3,5-Dii;RoM0iiETin'L 



-2-TOLUiDiNES. Also f,erhromides 



Csn3BrMe.NHMe.HBr.Br2 



and C6H2Br2Me.NHMe.HBr.Br2 



Fries, K. Liebigs Ann. Chem., Leip- 

 zig, 346, 1906, (128-219). 



Dimethyl-o-toluidine 



3,5-DlIlRuMuDIMEm\L-2-TOLUIDINE 



and the jjerhromidcs. 

 Fries, Iv. I.e. 



Dimetliyl-p toluidine 



3,5-Dir.ROMODIMETHYL-4-TOHJlWNE 



and the perbromide 

 C6H2Br2Me.NMe2.HBr.Br2. 

 Fries, K. I.e. 



TRIMETHYL-p-TOLYLAMMONIUil BROMIDE 



Perbromide MeC6H4.NMej.Br.Br2 

 Fries, K. I.e. 



Ethyl-/itoluidine 



3-Bro.mo and 3,5-pini!o.MnETiiYE- 

 -4-T0Lt:iDiNEs and tlie perbromide 

 CGH2Br2Me.NllEt.lIBr.Br2 

 Fries, K. I.e. 



Benzylamine C6H5.CH2.NH2 



Krauth, W. Para-Chlorphenylacet- 

 hvdrazid mid das Para-Chlorbenzylamin. 

 Diss. Heidelberg, 1904. 



